Identity
- Trade Name
- Medic Enhancement Set FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- The Medic Enhancement Set is convenience kit with a capability improvement providing a combination of advanced tools for the management of massive hemorrhage, airway compromise, respiratory system insults and circulatory compromise. • The set is comprised of color coded MARCH protocol devices for rapid visual identification of the appropriate tool required under the MARCH protocol. • Each set is designed to augment or enhance first respondents treatment capacities. TMT-Tourniquet 2 ea Celox Rapid 2 ea iTClamp 1 ea Control-Cric 1 ea Sentinel Chest Seal 2 ea TALON IO Starter Set 1 ea Battle Bandage 2 ea FDA UDI
- Model / Reference
- 01 FDA UDI
- Description
- The Medic Enhancement Set is convenience kit with a capability improvement providing a combination of advanced tools for the management of massive hemorrhage, airway compromise, respiratory system insults and circulatory compromise. • The set is comprised of color coded MARCH protocol devices for rapid visual identification of the appropriate tool required under the MARCH protocol. • Each set is designed to augment or enhance first respondents treatment capacities. TMT-Tourniquet 2 ea Celox Rapid 2 ea iTClamp 1 ea Control-Cric 1 ea Sentinel Chest Seal 2 ea TALON IO Starter Set 1 ea Battle Bandage 2 ea FDA UDI
Identifiers
- Catalog Number
- 82-504-03 FDA UDI
- Primary DI / UDI-DI
- M6988250403010 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
MR Unsafe FDA UDI
Category: First aid kit, non-medicated, single-use
Medic Enhancement Set by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as First aid kit, non-medicated, single-use.
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- 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 |
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Manufacturer
- Manufacturer
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI 43503066-4f7d-4f2c-a455-a2af91d7d07f 36 fields · synced May 30, 2026