Identity
- Trade Name
- Avitus Bone Harvester FDA UDI
- Generic Name
- Bone graft harvesting filter FDA UDI
- Device Name
- Sterile, disposable surgical instrument with 5mm cutting tip for large volume, cancellous bone and marrow harvesting with marrow separation insert. FDA UDI
- Model / Reference
- BH-210 FDA UDI
- Description
- Sterile, disposable surgical instrument with 5mm cutting tip for large volume, cancellous bone and marrow harvesting with marrow separation insert. FDA UDI
Identifiers
- Catalog Number
- BH-210 FDA UDI
- Primary DI / UDI-DI
- 00857373006036 FDA UDI
- FDA Product Code
- KNW FDA UDI
- GMDN Term
- Bone graft harvesting filter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1075 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
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: Neurosurgical curette, single-useBone graft harvesting filter
Avitus Bone Harvester by Avitus Orthopaedics, Inc — 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
- Avitus Orthopaedics, Inc
Sources (1)
- FDA UDI ac4f5f30-4bdb-426f-8a8c-11ab2a4e03e9 34 fields · synced May 30, 2026