Identity
- Trade Name
- Arthrex® FDA UDI
- Generic Name
- Blood centrifugation system FDA UDI
- Device Name
- ARTHREX ANGEL PRP KIT (US VERSION) FDA UDI
- Model / Reference
- ABS-10061 FDA UDI
- Description
- ARTHREX ANGEL PRP KIT (US VERSION) FDA UDI
Identifiers
- Catalog Number
- ABS-10061 FDA UDI
- Primary DI / UDI-DI
- 00888867083981 FDA UDI
- FDA Product Code
- ORG FDA UDI
- GMDN Term
- Blood centrifugation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9245 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
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: Blood centrifugation system
Arthrex® by Arthrex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Blood centrifugation system.
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
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
- Arthrex, Inc.
Sources (1)
- FDA UDI f7f7efea-a585-4841-ba4f-19d72213c188 35 fields · synced May 31, 2026