Healthcare-Related FAQs

Is a surgical mask an N95 respirator?

No. Surgical masks are not designed for use as particulate respirators and do not provide as much respiratory protection as an N95 respirator. Surgical masks provide barrier protection against droplets including large respiratory particles. Most surgical masks do not effectively filter small particles from the air and do not prevent leakage around the edge of the mask when the user inhales.2 The NIOSH Science Blog: N95 Respirators and Surgical Masks, posted 10/15/2009, provides an explanation of the science behind and the similarities/differences between NIOSH-approved particulate respirators and surgical masks.

2 Reference: Rengasamy,S., B.C.Eimer, and R.E.Shaffer. (2009) Filtration performance of FDA-Cleared surgical masks. Journal International Society Respiratory Protection 26; 54-70.

OSHA Video: The Difference Between Respirators and Surgical Masks (scroll down page)
The Difference Between Respirators and Surgical Masks. U.S. Department of Labor Video, (2009, December 16). This video is available in English and Spanish and is available for downloading.

What is a surgical N95 respirator?

A surgical N95 respirator is a NIOSH-approved N95 respirator that has also been cleared by the Food and Drug Administration (FDA) as a surgical mask. These products are noted in bold font on the table ofNIOSH-approved N95 respirators. For your convenience, a comprehensive table of these products appears below. If you have a product that you believe is FDA cleared that does not appear on this table, you should verify the FDA clearance by contacting the FDA at 1-800-638-2041.

The National Institute for Occupational Safety and Health (NIOSH) is the U.S. Government agency responsible for the certification and approval of respiratory protective devices for occupational use. The authority is granted to NIOSH in accordance with conditions and standards established in Title 42 of the Code of Federal Regulations (CFR), Part 84. It also addresses quality assurance requirements for the manufacturing of respiratory protective equipment. The approach to approval is that anybody can manufacture and sell any type of respiratory protective device, but only those that meet or exceed all of the requirements established in the 42 CFR 84 standards are acknowledged by NIOSH, and only those that have been NIOSH certified may be marketed as a NIOSH-approved respirator.

The Food and Drug Administration (FDA) is the U.S. Government agency that oversees most medical products, foods, and cosmetics. Within the FDA, the Center for Devices and Radiological Health (CDRH) oversees the safety and effectiveness of medical devices. Medical devices intended for use in preventing and treating disease is subject to regulation under the device provisions of the Federal Food, Drug, and Cosmetic Act. This includes surgical masks and surgical N95 respirators. The FDA has no role in the approval or clearance of N95 respirators not intended for use as a medical device.

This table of Surgical N95's is provided as a courtesy. If you have a product that you believe is FDA cleared that does not appear on this table, you should verify the FDA clearance by contacting the FDA at 1-800-638-2041.

Supplier/Manufacturer	Model/ Product	Approval  Number	User Donning Instructions
3M Company 888-3M HELPS	1860	84A-0006	Instructions
	1870	84A-3844	[PDF - 190 KB]
	1805	84A-5469	[PDF - 330 KB]
	1805S	84A-5470	[PDF - 330 KB]
Aearo Corporation 800-444-4774	Pleats Plus  N951050  1050S  1051  1051S  1052	84A-2630	[PDF - 205 KB]
	N9504C  N9504CS	84A-3715	[PDF - 14 KB]
	N9514C	84A-4272	[PDF - 14 KB]
	Pleats Plus  1054S  1054	84A-4320	[PDF - 205 KB]
Alpha Pro Tech 800-749-1363	MAS 695	84A-0457	[PDF - 211 KB]
Ansell Healthcare Products LLC [*W] 800-821-7236	112410	84A-5200	112410  [PDF - 759 KB]
	112411	84A-5201	112411  [PDF - 759 KB]
Cardinal Health [*E] 800-379-9929	N95-ML	84A-3323	[PDF - 842 KB]
	N95-S	84A-4107	[PDF - 5.6 MB]
	N95A-ML	84A-5411	[PDF - 538 KB]
	N95A-S	84A-5463	[PDF - 538 KB]
Cardinal Health [*Z]  866-401-8972	USA-N95-S	84A-5229	[PDF - 1.8 MB]
	USA-N95-R	84A-5527	[PDF - 3.2 MB]
Dynarex Corporation [*E] 800-379-9929	2295	84A-3323	[PDF - 842 KB]
	2296A	84A-4541	[PDF - 5.5 MB]
	2295A	84A-5411	[PDF - 538 KB]
Emerald Medical Inc. [*E] 610-670-8571	N9500	84A-3323	[PDF - 2.7 MB]
Filligent (HK) Limited 852-2542-2400	Professional BF-200-3013AN	84A-6252	Pending NIOSH receipt from company
Foss Manufacturing Company 603-929-6000	SpectraShield 9500	84A-5199	[PDF - 577 KB]
	Spectra Shield Protector N95	84A-5670	Spectra Shield Protector N95  [PDF - 577 KB]
GlaxoSmithCline Consumer Healthcare[*C] 800-821-7236	ActiProtect UF	84A-5163	[PDF - 59 KB]
Handen Heng Yong Protective and Clean Products Company, Ltd. 86-311-8551-8218 86-311-8551-8968	HY8510	84A-4276	[PDF - 105 KB]
	HY9810	84A-4521	[PDF - 114 KB]
Inovel, LLC [*J] 800-421-0668	1511  1512  1513  1517  Obsolete 08/2009	84A-0013	Instructions
Inovel, LLC 866-546-6835	FRN95-S  FRN95-ML  FRN95-A  FRN95-XS  Obsolete 05/2012	84A-4100	Instructions
	FRN95-SEZ  FRN95-MLEZ Obsolete 05/2012	84A-4101	Instructions
	3001N95-S  3002N95-M  3003N95-L  3004N95-LP Obsolete 05/2012	84A-4102	Instructions
	3101N95-S  3102N95-M/L Obsolete 05/2012	84A-4103	Instructions
	1510 Obsolete 05/2012	84A-4333	Instructions
	3211N95-S  321N95-M/L  3217N-95-LP Obsolete 05/2012	84A-4338	Instructions
Kimberly-Clark Corporation 800-524-3577	46827  46867	84A-0005	Instructions
	46727  46767	84A-0010	Instructions
Livingstone International Pty, Ltd. [*E] 800-379-9929	FMN95RN	84A-5411	[PDF - 538 KB]
Louis M. Gerson Company, Inc. 800-225-8623	1730	84A-0160	[PDF - 122 KB]
	2130 2131	84A-4123	[PDF - 122 KB]
Magid Glove and Safety, LLC [*E] 800-379-9929	910-N95	84A-3323	[PDF - 842 KB]
Makrite Industries, Inc. 800-379-9929	910-N95	84A-3323	[PDF - 842 KB]
	910-N95S	84A-4107	[PDF - 5.6 MB]
	910-N95FMX	84A-4541	[PDF - 5.6 MB]
	9500-N95	84A-5411	9500-N95  [PDF - 538 KB]
	9500-N95S	84A-5463	9500-N95S  [PDF - 615 KB]
Medline Industries, Inc. [*E] 800-379-9929	NON24506	84A-3323	[PDF - 842 KB]
	NON24507	84A-4107	[PDF - 5.6 MB]
	NON24506A	84A-5411	NON24506A  [PDF - 538 KB]
	NON24507A	84A-5463	NON24506A  [PDF - 538 KB]
Moldex-Metric, Inc. 800-421-0668	1511  1512  1513  1517	84A-0013	Instructions
	2210GN95-XS 2211GN95-S 2212GN95-M/L 2217GN95-LP	84A-4339	Instructions
	1510	84A-5171	Instructions
	3211N95-S 3212N95-ML 3217N95-LP	84A-5172	Instructions
	1712	84A-5227	[PDF - 127 KB]
Nexera Medical Inc. [*AA] 603-929-6000	SpectraShield 9500	84A-5199	SpectraShield 9500  [PDF - 577 KB]
	SpectraShield Protector N95	84A-5670	Spectra Shield Protector N95  [PDF - 577 KB]
Precept Medical Products [*E] 800-379-9929	65-3395	84A-3323	[PDF - 182 KB]
	65-3395S	84A-4107	[PDF - 182 KB]
Prestige Ameritech 866-401-8972	RP88020	84A-5216	[PDF - 256 KB]
	USA-N95-S	84A-5229	[PDF - 1.8 MB]
	RP88010	84A-5475	[PDF - 187 KB]
	USA-N95-R	84A-5527	[PDF - 3.2 MB]
priMed Medical Products Company 1-877-877-4633	PN4-7064 PN4-7074 PN4-7084	84A-5535	[PDF - 1.6 MB]
	PN4-7065 PN4-7075 PN4-7085	84A-6659	Pending NIOSH receipt from company
Shanghai Dasheng Health Products Manufacture Company, Ltd. 86-21-5778-3126	DTC3M-1	84A-4331	[PDF - 247 KB]
	DTC3B	84A-4336	[PDF - 247 KB]
Shanghai Gangkai Purifying Products Company, Ltd. 86-21-5777-5401	GIKO 1400	84A-4282	[PDF - 78 KB]
Shuenn Bao Shing Corporation 886-4-875-6141	AP0018 N95	84A-4049	[PDF - 63 KB]
	AP0028	84A-4175	[PDF - 65 KB]
Sperian Respiratory Protection USA, LLC 800-821-7236  800-343-3411	1930 Obsolete 04/2010	84A-0301	[PDF - 33 KB]
	1940 Obsolete 04/2010	84A-0301	[PDF - 594 KB]
	HC-NB095	84A-4357	[PDF - 33 KB]
	HC-NB295F	84A-4371	[PDF - 33 KB]
	HC-NB095F	84A-4372	[PDF - 33 KB]
	HC-NB295FP	84A-5667	Pending
SteelPro [*A] 800-225-8623	1730	84A-0160	1730  [PDF - 122 KB]
TrioMed Innovations Corporation 858-794-3200	B130	84A-5200	[PDF - 759 KB]
	B150	84A-5201	[PDF - 759 KB]
A - Private label of Louis M. Gerson Company, Inc. (800-225-8623) AA - Private label of Foss Manufacturing Company(603-929-6000) C - Private label of Sperian (800-821-7236) E - Private label of Makrite Industries, Inc. (800-749-1363) J - Private label of Moldex-Metric, Inc. (800-421-0668) W - Private Label of TrioMed Innovations Corporation (800-821-7236) Z - Private Label of Prestige Ameritech (866-401-8972)

Can the products with an exhalation valve be used in healthcare?

Respirators with exhalation valves can be used in a healthcare setting when it is not important to maintain a sterile field (an example of an acceptable practice would be when taking the temperature or blood pressure of a patient). Respirators with exhalation valves should not be used in situations where a sterile field is required (e.g. during an invasive procedure in an operating or procedure room) because the exhalation valve allows unfiltered exhaled air to escape into the sterile field.

Do N95 respirators come in different sizes?

Yes. The sizing differs with each respirator model. Some of the sizing options include small, small/medium, medium, medium/large, and large. Particulate filtering facepiece respirators, including those commonly referred to as N95s, are available in multiple size configurations that are variable and not standardized across models.

How do I know what size I need?

Fit testing is needed to determine if a particular size and model of respirator provides you with an acceptable fit. Fit testing is model specific. Before you wear a respirator in an occupational setting, youmust be fit tested in each respirator model you will wear.

Do N95 respirators come in different styles?

Yes. Filtering facepiece respirators are available in a wide range of colors, shapes, and styles. Some styles will fit individuals better than others and certain styles may be more comfortable and have better fitting characteristics. As long as the N95 is NIOSH-approved, has been fit tested, and is being used in accordance with the requirements of an OSHA-compliant respirator program, including appropriately donned by the user, then the wearer should receive the expected protection factor regardless of color, shape, or style.

Below are some of the styles available:

Photos courtesy of 3M, Kimberly-Clark, and Moldex.

Why do some N95 respirators have an exhalation valve on the front?

The use of an exhalation valve reduces exhalation resistance, which makes it easier to breathe (exhale). Some users feel that a respirator with an exhalation valve keeps the face cooler and reduces moisture build up inside the facepiece.

Does moisture build up in respirators?

The wearer’s respiratory secretions and moist exhaled breath can lead to moisture build-up in a respirator. While it is possible for moisture to build up in a respirator with or without an exhalation valve, preliminary research shows that this is unlikely.

What are the differences among these products?

Surgical, Medical, or Procedure Mask	N95 Respirator	Surgical N95 Respirator
Standard Earloop Mask Photo courtesy of Newton Safety/Sanax	Molded Cup Style N95 respirator Photo courtesy of Sperian	Molded Cup Style Surgical N95 respirator Photo courtesy of Sperian
Standard Tie On Surgical Mask Photo courtesy of Newton Safety/Sanax	Pleated style N95 respirator Photo courtesy of Alpha TechPro	Duck bill style Surgical N95 Photo courtesy of Kimberly Clark
Duckbill surgical mask	Flexwing style, one strap N95 respirator Photo courtesy of Moldex	Flexwing style, one strap, Duramesh cover Surgical N95 respirator Photo courtesy of Moldex
Molded Cone Surgical Mask Photo courtesy of 3M	Photo courtesy of 3M Cup Style and Flat Fold N95 Respirators Photo courtesy of Newton Safety/Sanax	Cup Style Surgical N95 respirator (interior and exterior view) Photo courtesy of Louis Gerson

Surgical, Medical, or Procedure Mask	N95 Respirator	Surgical N95 Respirator
Evaluation, Testing and Certification
Filter efficiency, breathing resistance, fluid resistance and flammability data are reviewed by the FDA. Must demonstrate filtration efficiency no less than another surgical mask already cleared by the FDA. (the minimum filtration level is unspecified).	Evaluated, tested and certified by NIOSH as per the minimum performance requirements like filter efficiency and breathing resistance. NIOSH approves 9 filter classes of which N95 is the lowest.	Evaluated, tested and certified by NIOSH as per the minimum performance requirements as an N95 filtering facepiece respirator. FDA accepts filter efficiency and breathing resistance based on NIOSH test results from the NIOSH approval evaluation, and reviews fluid resistance and flammability data submitted by the manufacturer for clearance of the N95 respirator as a medical device for use in a surgical setting.
Intended Use
A surgical mask is intended to prevent the release of potential contaminants from the user into their immediate environment. It is also used to protect the wearer from large droplets, sprays and splashes of body fluids.	Occupational (including medical) use. Reduces wearer’s exposure to particles including small particle aerosols and large droplets (all non-oil aerosols).	Can be used in any occupational setting where an N95 respirator is appropriate. Medical use where a sterile field needs to be maintained. Reduces wearer’s exposure to certain airborne particles (all non-oil aerosols) and provides a barrier to splashes and sprays.
Purpose
Barrier to splash, droplets, spit.	Protects from exposure to airborne particles. In a healthcare setting, protects from exposure to biological aerosols including viruses and bacteria.	Protects from exposure to airborne particles and barrier to splashes, droplets, and sprays. In a healthcare setting, protects from exposure to biohazards including viruses and bacteria.
Face Seal Fit
Not designed to fit tight to face.	Designed to fit tight to face creating a seal around the perimeter of the respirator to improve protection.	Designed to fit tight to face creating a seal around the perimeter of the respirator to improve protection.
User Seal Check Requirement
Not designed for seal check.	Required each time a respirator is donned.	Required each time a respirator is donned.
Filtration
Does not effectively filter small particles from air.	Effectively filters large and small particles from air.	Effectively filters large and small particles from air.
Leakage
Leakage occurs around the edge of the mask when the user inhales.	When properly fitted and donned, minimal leakage around edges of the respirator when the user inhales.	When properly fitted and donned, minimal leakage around edges of the respirator when the user inhales.
Use Limitations
One time use (one patient encounter).	Single use. Should be discarded when it becomes damaged or deformed; no longer forms an effective seal to the face; becomes wet or visibly dirty; breathing through it becomes more difficult; or if it becomes contaminated with blood, respiratory or nasal secretions, or other bodily fluids from patients.	Single use. Should be discarded when it becomes damaged or deformed; no longer forms an effective seal to the face; becomes wet or visibly dirty; breathing through it becomes more difficult; or if it becomes contaminated with blood, respiratory or nasal secretions, or other bodily fluids from patients.
Available sizes
Generally only one size.	Available in multiple size configurations. However, sizing is not standardized among approved models. Some of the sizing options include small, small/medium, medium, medium/large, and large.	Available in multiple size configurations. However, sizing is not standardized among approved models. Some of the sizing options include small, small/medium, medium, medium/large, and large.

How long can you wear the same N95 respirator?

The current NIOSH service-time-limit recommendations for non-powered particulate filter respirators are that filter elements should be replaced at the following frequencies:

• The service life of all filters on NIOSH-approved respirators is limited by considerations of hygiene, damage, and breathing resistance. All filters should be replaced whenever they are damaged, soiled, or causing noticeably increased breathing resistance.
• N-series filters generally should be used and reused subject only to considerations of hygiene, damage, and increased breathing resistance. However, for dirty workplaces that could result in high filter loading (i.e., 200 mg), service time for N-series filters should only be extended beyond 8 hours of use (continuous or intermittent) by performing an evaluation in specific workplace settings that demonstrates: (a) that extended use will not degrade the filter efficiency below the efficiency level specified in 42 CFR 84, or (b) that the total mass loading of the filter(s) is less than 200 mg. These determinations would need to be repeated whenever conditions change or modifications are made to processes that could change the type of particulate generated in the user's facility.
• For healthcare applications where use is for protection against confirmed or suspected 2009 H1N1 influenza, please refer to: Interim Guidance on Infection Control Measures for 2009 H1N1 Influenza in Healthcare Settings, Including Protection of Healthcare Personnel.

Can a N95 respirator be used from Operating Room (OR) case to OR case or from patient to patient?

Used respirators are considered contaminated and ideally should be discarded after each patient encounter. Disposable N95 respirators worn during aerosol-generating procedures should be discarded after the procedure.

Healthcare facilities can extend the use of disposable N95 respirators by training personnel to wear them during serial patient encounters without removing or re-donning between encounters. There is the risk of respirator contamination and contact transmission with this practice where extended use of disposable N95 respirators could entail a risk of contact transmission by touching a contaminated surface of the respirator and subsequently touching the mucous membranes of the face or a hypothetical risk of re-aerosolization of virus from a used respirator. The risk will be minimized if HCWs perform hand hygiene every time before and after touching the respirator.

For healthcare applications where use is for protection against confirmed or suspected 2009 H1N1, please refer to Interim Guidance on Infection Control Measures for 2009 H1N1 Influenza in Healthcare Settings, Including Protection of Healthcare Personnel and Questions & Answers Regarding Respiratory Protection for Infection Control Measures for 2009 H1N1 Influenza among Healthcare Personnel for recommendations for the duration of wear for protection against the 2009 H1N1 exposure hazards.

Is cross contamination a concern if I wear the same N95 from patient room to patient room?

Yes, especially if the respirator was worn in a room with any type of aerosol generating procedure, or if the patient is suspected of or confirmed with having the 2009 H1N1 virus. Although this practice has the potential benefit of providing respiratory protection with limited supplies of respirators, there is the risk of respirator contamination and contact transmission. Extended use (i.e. use without removing or re-donning between encounters) of disposable N95 respirators could entail a risk of contact transmission by touching a contaminated surface of the respirator and subsequently touching the mucous membranes of the face or a hypothetical risk of re-aerosolization of virus from a used respirator. The precise balance between risk of contact transmission and benefit of extended use is unknown, although the risk will be minimized if HCWs perform hand hygiene every time before and after touching the respirator. In general, wearing an N95 respirator over multiple encounters (while minimizing touching, removing, or re-donning between encounters) would be favored over re-use, as this strategy is expected to involve less touching of the respirator and therefore less risk of contact transmission. For healthcare applications where use is for protection against confirmed or suspected 2009 H1N1, please refer toInterim Guidance on Infection Control Measures for 2009 H1N1 Influenza in Healthcare Settings, Including Protection of Healthcare Personnel and Questions & Answers Regarding Respiratory Protection for Infection Control Measures for 2009 H1N1 Influenza among Healthcare Personnel for recommendations for the duration of wear for protection against the 2009 H1N1 exposure hazards.

Can I take a N95 respirator off in between patients or Operating Room cases?

Used respirators are considered contaminated and ideally should be discarded after each patient encounter. A user should never touch the contaminated front of the respirator with his or her bare hands. Hands should always be washed after donning and doffing the respirator. Healthcare facilities implementing steps to extend the existing supply of disposable N95 respirators by training personnel to re-use them (i.e. removing and re-donning between patient encounters) refer to Questions & Answers Regarding Respiratory Protection for Infection Control Measures for 2009 H1N1 Influenza among Healthcare Personnel for recommendations for the possible re-use of respirators between patient encounters when used for protection against the 2009 H1N1 exposure hazards.

How should I store my N95 in between patient encounters, in a healthcare setting?

The manufacturers provide instructions for cleaning, sanitizing, repairing, inspecting, and storing their respirators. The respirators should be packed or stored so that the respirators do not become damaged or deformed. Never store disposable respirators in pockets, plastic bags, or other confined areas. Infectious material deposited on personal protective equipment may cause it to become a vehicle for direct or indirect transmission. In those situations, care is needed when removing and storing personal protective equipment to avoid contaminating skin, clothing, and mucous membranes. Remove the respirator and either hang it in a designated area or place it in a bag. (Consider labeling respirators with a user’s name before use to prevent reuse by another individual.) In healthcare settings where the patients have confirmed or suspected 2009 H1N1 influenza, please refer to Questions & Answers Regarding Respiratory Protection for Infection Control Measures for 2009 H1N1 Influenza among Healthcare Personnel for recommendations for the possible storage of respirators between patient encounters when used for protection against the 2009 H1N1 exposure hazards.

Can I infect myself from the droplets that accumulate on the outside of the respirator?

Respirators protect by capturing particles with the filter of the N95 respirator. Some aerosols can pose a contact hazard for infection. The accumulation of particles on the external surface of the respirator may be an exposure hazard from contact with the filter, including becoming a fomite for infectious agents. Users should be cautious and follow appropriate procedures to avoid self-inoculation from contact with these surfaces. Hand hygiene and infection control practices should be followed before and after touching the outside of the respirator when it is used in the presence of infectious agents.

Do I need special training to wear an N95 or do I put it on and wear it like a surgical mask?

The NIOSH certification requires respirators to be put on, used and maintained in accordance with the manufacturer instructions and a respiratory protection program that meets the requirements of the OSHA respiratory protection standard (29 CFR 1910.134). Training for all users is a mandatory part of OSHA’s respirator program requirements. Training is usually done at the same time that fit testing takes place. The OSHA standard contains required training elements. The manufacturer instructions for donning and doffing for each brand and model may be model-specific and must be followed. These instructions are located in the User Instructions provided, on the box or individual package of the respirators. The manufacturer’s instruction for putting on (donning) the respirator is also included in the information provided in the NIOSH listing for approved disposable respirators.

Can we use an N95 that has not been cleared by the FDA in a patient setting?

NIOSH-certified N95 respirators that have not been cleared by the FDA can be used for respiratory protection to reduce the exposures of healthcare personnel in a patient setting to hazardous particulates. These respirators have not been evaluated by FDA to determine whether they meet the fluid and flammability resistance as required for FDA clearance as medical devices. For this reason, they are not intended for use in exposure settings where the performance of a surgical mask to maintain a sterile field is required.

What does it mean if a respirator is approved by NIOSH and cleared by the FDA?

N95 respirators that are both certified by NIOSH and cleared by FDA as medical devices for use by healthcare personnel are called “surgical N95 respirators.” As with all NIOSH-certified N95 respirators, these products have been evaluated by NIOSH certification process and have demonstrated that they can filter out a minimum of 95% of airborne particles under worse case test conditions. These products have also been evaluated by the FDA to have demonstrated an acceptable level of fluid and flame resistance, which may be important in healthcare occupational settings, such as surgical suites. The FDA clearance process also requires that these products have labeling that is relevant to healthcare personnel, such as information about the presence of natural rubber latex.