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Sizer Set - for Use with Osteochondral Allograft, PRE-CUT CORE
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Sizer Set - for Use with Osteochondral Allograft, PRE-CUT CORE FDA UDI
- Generic Name
- Orthopaedic implant-instrument extension adaptor, single-use FDA UDI
- Device Name
- OCA Single-Use Sizer Set FDA UDI
- Model / Reference
- PKG-90-AOI-000002 FDA UDI
- Description
- OCA Single-Use Sizer Set FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860010346938 FDA UDI
- FDA Product Code
- QBO FDA UDI
- GMDN Term
- Orthopaedic implant-instrument extension adaptor, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.4505 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
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
Yes
FDA UDI
Category: Orthopaedic implant-instrument extension adaptor, single-use
Sizer Set - for Use with Osteochondral Allograft, PRE-CUT CORE by Swami Medical — 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
- Swami Medical
Sources (1)
- FDA UDI 1208ed40-3b0b-48b2-997f-8506db1dad6a 33 fields · synced May 30, 2026