Ran-132 13 Ga X 2 in
by Ranfac Corp.
Ran-132 13 Ga X 2 in is a Class II device made by Ranfac Corp., cleared under FDA 510(k) K131157 on 22 Oct 2013 and listed in FDA GUDID since 14 Feb 2023 (UDI-DI 00850023741745), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850023741745 | Date14 Feb 2023 | StatusListed |
| United States | FDA 510(k) | NumberK131157 | Date22 Oct 2013 | StatusActive |
Official records
- AccessGUDID record 00850023741745
- FDA 510(k) database K131157
Across registries
- FDA 510(k) K131157 decided 22 Oct 2013 Active
- FDA GUDID UDI-DI 00850023741745 listed 14 Feb 2023 Listed
Timeline
- Cleared FDA 510(k) K131157
- Listed FDA GUDID 00850023741745
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ran-132
- Generic name
- Bone access cannula
- Model / Ref / Catalog
- 13 GA X 2 IN, RAN-132
- Primary DI / UDI-DI
- 00850023741745
- 510(k) Number
- FDA product code
- KNW
- GMDN term
- Bone access cannula
- Device class
- Class II
- Regulation number
- 876.1075
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 2 InchNeedle Gauge — 13 Gauge
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