Identity
- Trade Name
- IFAK RESUPPLY FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- IFAK Resupply is designed to be used under the most adverse conditions. It uses medical gear in a color-coded trauma treatment system to treat the leading causes of preventable death in combat situations. FDA UDI
- Model / Reference
- 05 FDA UDI
- Description
- IFAK Resupply is designed to be used under the most adverse conditions. It uses medical gear in a color-coded trauma treatment system to treat the leading causes of preventable death in combat situations. FDA UDI
Identifiers
- Catalog Number
- 81-201-01 FDA UDI
- Primary DI / UDI-DI
- M6898120101050 FDA UDI
- FDA Product Code
- OHO FDA UDI
- GMDN Term
- First aid kit, non-medicated, 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, non-medicated, single-use
Ifak Resupply by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI 832420ba-4b67-4f5c-989a-4a1b0f61d528 35 fields · synced Jun 1, 2026