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Sign in to claim this brandNHAT QUANG INDUSTRY COOPERATIVE
US
Last updated May 31, 2026
What NHAT QUANG INDUSTRY COOPERATIVE makes
NHAT QUANG INDUSTRY COOPERATIVE manufactures single-use public respirator masks, designed for general respiratory protection in public settings. The VINMASK is a key product in this category, intended for disposable use to filter airborne particles.
The company’s respirator products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The cooperative operates in the United States, adhering to applicable U.S. medical device compliance requirements.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does NHAT QUANG INDUSTRY COOPERATIVE primarily manufacture?
NHAT QUANG INDUSTRY COOPERATIVE specializes in single-use public respirator masks, such as the VINMASK. These devices are designed for disposable respiratory protection in public environments, filtering airborne particles to reduce exposure to contaminants.
Where is NHAT QUANG INDUSTRY COOPERATIVE based, and what regulatory framework applies to its devices?
The company is based in the United States. Its respirator products, including the VINMASK, are classified under FDA Class II, meaning they undergo stricter regulatory oversight due to their role in protecting users from airborne hazards. Compliance with U.S. medical device regulations applies.
Are NHAT QUANG INDUSTRY COOPERATIVE’s devices listed in any regulatory registries?
Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices like the VINMASK, ensuring transparency and traceability for regulatory and market purposes.
How are NHAT QUANG INDUSTRY COOPERATIVE’s respirator devices classified by regulatory authorities?
The company’s single-use public respirators, such as the VINMASK, fall under FDA Class II classification. This classification is assigned based on the device’s risk level—Class II devices require special controls beyond general controls to ensure safety and effectiveness, reflecting their critical role in respiratory protection.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 555329738
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vinmask | 1 | FDA UDI | Class II | Active |
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