0306195000
0306195000 (0306-195-000) is a Class II device made by Stryker Corp., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04546540898920), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04546540898920 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04546540898920
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Vertebral bone biopsy procedure kit, single-use
- Model / Ref / Catalog
- 0306195000, 0306-195-000
- Primary DI / UDI-DI
- 04546540898920
- FDA product code
- KNW
- GMDN term
- Vertebral bone biopsy procedure kit, single-use
- Device class
- Class II
- Regulation number
- 876.1075
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 9.0 InchNeedle Gauge — 10.0 Gauge
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