Identity
- Trade Name
- MACI Arthroscopic Instruments FDA UDI
- Generic Name
- Bone curette, single-use FDA UDI
- Device Name
- 12 mm x 21 mm Min arthroscopic cutter FDA UDI
- Model / Reference
- 82025 FDA UDI
- Description
- 12 mm x 21 mm Min arthroscopic cutter FDA UDI
Identifiers
- Catalog Number
- N/A FDA UDI
- Primary DI / UDI-DI
- 00860004093046 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Bone curette, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bone curette, single-use
MACI Arthroscopic Instruments by Vericel Corporation — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Vericel Corporation
Sources (1)
- FDA UDI e7fe88c2-81ea-478e-96db-2ac2dc04acb2 34 fields · synced Jun 1, 2026