GTDI item MR-1201
N95 respirator, welded headbands, 160 per case
- NIOSH Approved N95
NIOSH Approved N95 filtering facepiece respirator for industrial and occupational use, with no exhalation valve, ultrasonically welded thermoplastic elastomer headbands, an adjustable aluminum nose clip and polyurethane nose foam; standard size. The manufacturer states no FDA clearance as a surgical mask. Shelf life five years from the date of manufacture; contains no components made from natural rubber latex, as stated. Made in the USA with globally sourced materials, as stated by the manufacturer. 20 respirators per box, 8 boxes (160) per case. Fit testing is model specific; your quote names the exact model.
Specifications
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| Attribute | Value | Basis |
|---|---|---|
| Identity and regulatory status | ||
| GTDI item code | MR-1201 | Internal |
| Regulatory status | NIOSH Approved N95 filtering facepiece respirator. The manufacturer states no FDA clearance as a surgical mask. The TC approval number is on your quote. | The product's own clearance, approval or registration |
| NIOSH filter class | N95 | Regulator record |
| FDA clearance as a surgical mask | No. The manufacturer states no FDA clearance as a surgical mask. | Manufacturer specification |
| Intended use (as stated) | For industrial and occupational use only; not for consumer sale or use, as stated by the manufacturer | Manufacturer specification |
| NIOSH approval | NIOSH Approved N95. The TC approval number is on your quote so you can confirm it in NIOSH's list of approved respirators. | Regulator record |
| Material and construction | ||
| Exhalation valve | No | Manufacturer specification |
| Straps | Ultrasonically welded headbands; straps to thermoplastic elastomer | Manufacturer specification |
| Strap attachment | Two-strap design with welded dual point attachment | Manufacturer specification |
| Nose clip and foam | Adjustable nose clip (aluminum); nose foam (polyurethane) | Manufacturer specification |
| Materials | Filter to polypropylene; shell to polyester; coverweb to polyester | Manufacturer specification |
| Size | Standard | Manufacturer specification |
| Performance, testing and labeling | ||
| Assigned protection factor | APF 10, as stated by the manufacturer | Manufacturer specification |
| Natural rubber latex | Contains no components made from natural rubber latex, as stated by the manufacturer | Manufacturer specification |
| Fit test | Fit testing is model-specific. Tell us the model your staff are fit-tested to. Your quote confirms that exact model or names an alternative for your approval. | 29 CFR 1910.134 |
| Storage, origin and packaging | ||
| Shelf life | 5 years from the date of manufacture | Manufacturer specification |
| Storage | Store in temperatures between -4°F (-20°C) and +86°F (+30°C) and not exceeding 80% RH | Manufacturer specification |
| Country of origin (as stated) | Made in the USA with globally sourced materials, as stated by the manufacturer | Manufacturer specification |
| Packaging | 20 respirators per box, 8 boxes per case | Manufacturer specification |
Sizes and packaging
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| Size or variant | Variant code | Respirators per pack | Packs per case | Respirators per case |
|---|---|---|---|---|
| Standard | MR-1201-STD | 20 | 8 | 160 |
Standards, testing and claims
- NIOSH Approved N95
- NIOSH Approved N95. The TC approval number is on your quote so you can confirm it in NIOSH's list of approved respirators.Basis: NIOSH approval record; the TC number is stated on your quote
- Manufacturer statement
- NIOSH Approved for at least 95% filtration efficiency against certain particles that do not contain oil, as stated by the manufacturer.Basis: As stated by the manufacturer; the document is supplied with the quote
- Manufacturer statement
- Meets the NIOSH 42 CFR part 84 N95 requirement of at least 95% filtration efficiency.Basis: As stated by the manufacturer; the document is supplied with the quote
- Manufacturer statement
- For industrial and occupational use only. Not for consumer sale or use.Basis: As stated by the manufacturer; the document is supplied with the quote
NIOSH Approved N95 filtering facepiece respirator. The manufacturer states no FDA clearance as a surgical mask. The TC approval number is on your quote.
Provided with your quote
- Spec sheet Supplied with your written quote, before you order With the quote
- NIOSH Certified Equipment List entry Supplied with your written quote, before you order With the quote
We substitute only with your written approval. A change of manufacturer counts as a substitution.
Compare with other n95 respirators
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| Product | Type | Shape | Sizes | Exhalation valve | Per box |
|---|---|---|---|---|---|
| N95 respirator, 160 per caseGTDI item MR-1201, this page | Standard | No | 20 | ||
| Surgical N95 respirator, 240 per caseGTDI item MR-1202 | N95, Surgical | Collapse resistant double-shell construction | One size, 20 per box | No | 20 |
| N95 respirator, molded shellGTDI item MR-1203 | Molded outer shell | Medium/large; small; a third size as labeled by the manufacturer, confirmed on your quote | No exhalation valve | 20 | |
| Surgical N95 respirator, cup styleGTDI item MR-1204 | N95, Surgical | Cup style, collapse resistant | Standard; small | No | 20 |
| Surgical N95 respirator, flat foldGTDI item MR-1205 | N95, Surgical | Three-panel flat fold | One size, 20 per box | No | 20 |
| Surgical N95 respirator, pouch styleGTDI item MR-1206 | N95, Surgical | Pouch style (expanded chamber) | Regular; small | No | 35 |
Questions buyers ask about masks and respirators
- Tell us the model your staff are fit-tested to. The quote confirms that exact model or names an alternative for your approval.
- Valved models are not for sterile fields. Surgical N95 models are always unvalved.
- Past its shelf life a respirator is no longer NIOSH Approved. Rotate stock by date.
Do we need a fluid barrier or airborne protection?
A mask protects against splashes and large droplets and is an FDA device under 21 CFR 878.4040. A respirator filters airborne particles and is approved by NIOSH under 42 CFR part 84. The task decides which, and the two are never interchangeable.
Which ASTM level suits which task?
ASTM F2100 rates masks at Level 1, 2 or 3 on bacterial and particulate filtration, breathability and resistance to synthetic blood at 80, 120 or 160 mmHg. Higher fluid resistance suits procedures with splash risk. Each listing shows the level and the test values behind it, as the edition on the manufacturer's test report states them.
Is this respirator NIOSH Approved, and how do we check?
Every respirator listed as N95 holds a current NIOSH approval. The TC approval number is on your quote so you can confirm it on the NIOSH Certified Equipment List. NIOSH treats "N95" and "NIOSH Approved" as registered certification marks, and a product without an approval may not carry them.
Surgical N95 or standard N95?
A surgical N95 is a NIOSH Approved respirator that is also fluid resistant and regulated by FDA as a Class II device. It is unvalved and states its fluid resistance level. A standard N95 is NIOSH Approved only. Sterile fields and procedure rooms call for the surgical version.
Is this the model our staff are fit-tested to?
Fit testing applies to the make, model, style and size tested. Tell us the model your staff are fit-tested to. Your quote confirms that exact model or names an alternative for your approval, and nothing is substituted without it.
What is the shelf life, and how do we rotate a stockpile?
Manufacturers set a shelf life, often about five years. Past its shelf life a respirator is no longer NIOSH Approved. Each listing shows the shelf life as stated, and quotes state the dating at shipment, so a stockpile can be rotated by date.
When is a KN95 acceptable?
A KN95 is made to China's GB 2626 standard and is not NIOSH Approved. It is listed plainly as such and is not for use where a NIOSH Approved respirator is required.
Related products
More sub-categories in masks and respirators.
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