Identity
- Trade Name
- MEDIC ENHANCEMENT RESUPPLY FDA UDI
- Generic Name
- Intraosseous infusion kit FDA UDI
- Device Name
- The Medic Enhancement Resupply provides advanced capabilities for the management of battlefield trauma, setting it apart from the standard issue medical equipment. Its increased capability is specifically designed to treat the five leading causes of preventable traumatic death in combat. The Medic Enhancement Resupply uses MARCH™ medical gear in a comprehensive, color-coded trauma treatment system distinctly packaged with icon identifiers for ease of access and identification. It is packaged in a rugged, vacuum sealed, nylon pouch providing a layer of protection to the components until needed. RXONLY FDA UDI
- Model / Reference
- 06 FDA UDI
- Description
- The Medic Enhancement Resupply provides advanced capabilities for the management of battlefield trauma, setting it apart from the standard issue medical equipment. Its increased capability is specifically designed to treat the five leading causes of preventable traumatic death in combat. The Medic Enhancement Resupply uses MARCH™ medical gear in a comprehensive, color-coded trauma treatment system distinctly packaged with icon identifiers for ease of access and identification. It is packaged in a rugged, vacuum sealed, nylon pouch providing a layer of protection to the components until needed. RXONLY FDA UDI
Identifiers
- Catalog Number
- 82-504-05 FDA UDI
- Primary DI / UDI-DI
- M6898250405060 FDA UDI
- FDA Product Code
- FMI FDA UDI
- GMDN Term
- Intraosseous infusion kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 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: Intraosseous infusion kit
Medic Enhancement Resupply by Safeguard Us Operating, Llc — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI 162f83f8-93ba-484a-b689-f116f9a37c4a 35 fields · synced Jun 8, 2026