GTDI item MR-1203
N95 respirator, molded shell, three sizes
- NIOSH Approved N95
NIOSH Approved N95 filtering facepiece respirator with a molded outer shell that the manufacturer states resists collapsing in hot, humid conditions, a molded nose bridge without a metal nose band, a soft foam nose cushion and a soft inner lining; no exhalation valve. Available in three sizes, including medium/large and small. The manufacturer states no FDA clearance as a surgical mask, a nine-year shelf life, heat and flame resistance under ANSI/ISEA 110-2009 section 7.11.1, and that the head straps contain natural rubber latex. Made in the United States, as stated by the manufacturer. 20 respirators per box, 12 boxes 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-1203 | 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 |
| NIOSH approval | NIOSH Approved N95. The TC approval numbers are on your quote so you can confirm them in NIOSH's list of approved respirators. | Regulator record |
| Material and construction | ||
| Exhalation valve | No exhalation valve | Regulator record |
| Shell | Molded outer shell | Manufacturer specification |
| Nose bridge and cushion | Molded pinch free nose bridge without a metal nose band; soft foam nose cushion | Manufacturer specification |
| Lining | Soft inner lining | Manufacturer specification |
| Sizes | Medium/large; small; a third size as labeled by the manufacturer, confirmed on your quote | Manufacturer specification |
| Performance, testing and labeling | ||
| Heat and flame resistance | Meets heat and flame resistance in accordance with ANSI/ISEA 110-2009 Section 7.11.1. | Manufacturer specification |
| PVC | PVC-free, as stated by the manufacturer | Manufacturer specification |
| Natural rubber latex | Contains natural rubber latex (head straps), as stated by the manufacturer | Manufacturer specification |
| Latex caution | Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions. | 21 CFR 801.437 |
| 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 | 9 Years | Manufacturer specification |
| Country of origin | United States, as stated by the manufacturer | Manufacturer specification |
| Packaging | 20 respirators per box, 12 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 |
|---|---|---|---|---|
| Medium/large | MR-1203-ML | 20 | 12 | 240 |
| Small | MR-1203-S | 20 | 12 | 240 |
| Third size, as labeled by the manufacturer (confirmed on your quote) | MR-1203-LP | 20 | 12 | 240 |
Standards, testing and claims
- NIOSH Approved N95
- NIOSH Approved N95. The TC approval numbers are on your quote so you can confirm them in NIOSH's list of approved respirators.Basis: NIOSH approval record; the TC number is stated on your quote
- Manufacturer statement
- The shell resists collapsing in hot, humid environments, as stated by the manufacturer.Basis: As stated by the manufacturer; the document is supplied with the quote
- Manufacturer statement
- Approved by NIOSH under 42 CFR part 84.Basis: As stated by the manufacturer; the document is supplied with the quote
- Manufacturer statement
- Persons highly sensitive to natural rubber latex may have an allergic reaction (manufacturer's caution).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, molded shellGTDI item MR-1203, this page | Molded outer shell | Medium/large; small; a third size as labeled by the manufacturer, confirmed on your quote | No exhalation valve | 20 | |
| N95 respirator, 160 per caseGTDI item MR-1201 | 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 |
| 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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