Identity
- Trade Name
- MARCH IFAK RESUPPLY FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- The MARCH™ IFAK Resupply bundle is intended to be used as resupply for the US Army standard IFAK or similar commercial applications. Using the combat-proven practice of kit organization and standardization, the MARCH™ IFAK Resupply is designed to be used under the most adverse conditions. It uses MARCH™ medical gear in a color-coded trauma treatment system to treat the five leading causes of preventable death on the battlefield. It comes with quick reference cards to complete the system. FDA UDI
- Model / Reference
- 12 FDA UDI
- Description
- The MARCH™ IFAK Resupply bundle is intended to be used as resupply for the US Army standard IFAK or similar commercial applications. Using the combat-proven practice of kit organization and standardization, the MARCH™ IFAK Resupply is designed to be used under the most adverse conditions. It uses MARCH™ medical gear in a color-coded trauma treatment system to treat the five leading causes of preventable death on the battlefield. It comes with quick reference cards to complete the system. FDA UDI
Identifiers
- Catalog Number
- 81-303-01 FDA UDI
- Primary DI / UDI-DI
- M6898130301120 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, non-medicated, single-use
March Ifak Resupply by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as First aid kit, non-medicated, single-use.
- IFAK — FARETEC, INC. · Class I
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
- Forward Tac-FAK Massive Hemorrhage (Tac-FAK M) — INTEGRATED MEDCRAFT LLC · Class I
- NAR — NORTH AMERICAN RESCUE, LLC.
- NAR Kit — NORTH AMERICAN RESCUE, LLC.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI 210136ab-8c5a-40e4-b431-4544bc0462c7 34 fields · synced Jun 1, 2026