Identity
- Trade Name
- TMM-PPE, Basic FDA UDI
- Generic Name
- Surgical/medical face mask, single-use FDA UDI
- Device Name
- Tactical Medical Module - Personal Protective Equipment, Basic FDA UDI
- Model / Reference
- 01456 FDA UDI
- Description
- Tactical Medical Module - Personal Protective Equipment, Basic FDA UDI
Identifiers
- Catalog Number
- 01456 FDA UDI
- Primary DI / UDI-DI
- 00856767008205 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, Basic by Altitude Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
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 bb1f4b20-eefa-47e9-8fd6-2f9d1d17ac40 34 fields · synced May 30, 2026