Identity
- Trade Name
- Adventure Medical Kits FDA UDI
- Generic Name
- Non-organic haemostatic agent FDA UDI
- Device Name
- 50 Person 2009 ANSI w/Eyewash Plstc FAK FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 50 Person 2009 ANSI w/Eyewash Plstc FAK FDA UDI
Identifiers
- Catalog Number
- 9999-2130 FDA UDI
- Primary DI / UDI-DI
- 00814471019306 FDA UDI
- FDA Product Code
- FRO FDA UDI
- GMDN Term
- Non-organic haemostatic agent FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
Yes
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
Yes
FDA UDI
Category: Non-organic haemostatic agent
Adventure Medical Kits by Adventure Ready Brands — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Adventure Ready Brands
Sources (1)
- FDA UDI ea7d7a84-ba7c-4cc4-82f8-70575171f885 35 fields · synced May 30, 2026