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Medic Enhancement Resupply

FDA UDI

Class II (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
MEDIC ENHANCEMENT RESUPPLY FDA UDI
Generic Name
Intraosseous infusion kit FDA UDI
Device Name
TMT - Tourniquet 4 ea Celox RAPID 4 ea Control-Cric 1 ea igel SGA (Size 5) 1 ea Nasal Trumpet 3 ea Sentinel Chest Seal 6 ea Dart 14g Needle/Catheter 3 ea TALON IO Start Set 1 ea Battle Bandage 3 ea HAWK Advanced Hypothermia Management Set 1 ea Eye Shield 2 ea Trauma Shears 1 ea TCCC Card (DD-1300 2 ea Permanent Marker 1 ea RXONLY FDA UDI
Model / Reference
00 FDA UDI
Description
TMT - Tourniquet 4 ea Celox RAPID 4 ea Control-Cric 1 ea igel SGA (Size 5) 1 ea Nasal Trumpet 3 ea Sentinel Chest Seal 6 ea Dart 14g Needle/Catheter 3 ea TALON IO Start Set 1 ea Battle Bandage 3 ea HAWK Advanced Hypothermia Management Set 1 ea Eye Shield 2 ea Trauma Shears 1 ea TCCC Card (DD-1300 2 ea Permanent Marker 1 ea RXONLY FDA UDI

Identifiers

Catalog Number
82-504-05 FDA UDI
Primary DI / UDI-DI
M6898250405000 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
Not 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
MRI Safety
MR Unsafe FDA UDI

Medic Enhancement Resupply by Safeguard Us Operating, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d1aace2e-0b98-40bb-8566-c415e1746abd 36 fields · synced Jun 1, 2026