Identity
- Trade Name
- TMM-PPE, Advanced FDA UDI
- Generic Name
- Surgical/medical face mask, single-use FDA UDI
- Device Name
- Chinook designed TMM-PPE Kit, Advanced (Tactical Medical Module-Personal Protective Equipment Kit, Advanced) with clothing and gear to provide barriers between you and a patient thus helping to prevent the spread of infection or illness. This kit contains the essential items necessary to protect your hands, clothes, face and lungs from splattered body fluids and airborne particles. FDA UDI
- Model / Reference
- 01457 FDA UDI
- Description
- Chinook designed TMM-PPE Kit, Advanced (Tactical Medical Module-Personal Protective Equipment Kit, Advanced) with clothing and gear to provide barriers between you and a patient thus helping to prevent the spread of infection or illness. This kit contains the essential items necessary to protect your hands, clothes, face and lungs from splattered body fluids and airborne particles. FDA UDI
Identifiers
- Catalog Number
- 01457 FDA UDI
- Primary DI / UDI-DI
- 00856767008229 FDA UDI
- FDA Product Code
- OHO FDA UDI
- GMDN Term
- Surgical/medical face mask, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical/medical face mask, single-use
TMM-PPE, Advanced by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical/medical face mask, single-use.
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- Precept® — Precept Medical Products, Inc. · Class II
- Precept® — Precept Medical Products, Inc. · Class II
- Surgical Face Mask — Foshan Nanhai Plus Medical Co., Ltd · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Altitude Technologies Inc.
Sources (1)
- FDA UDI 1afd06a9-edda-44e2-a355-7a38d6bd41bf 34 fields · synced Jun 8, 2026