MC-RAN-13FA 13 Gauge x 5in
by Ranfac Corp.
MC-RAN-13FA 13 Gauge x 5in 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 20 May 2021 (UDI-DI 00850023741202), 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 | Number00850023741202 | Date20 May 2021 | StatusListed |
| United States | FDA 510(k) | NumberK131157 | Date22 Oct 2013 | StatusActive |
Official records
- AccessGUDID record 00850023741202
- FDA 510(k) database K131157
Across registries
- FDA 510(k) K131157 decided 22 Oct 2013 Active
- FDA GUDID UDI-DI 00850023741202 listed 20 May 2021 Listed
Timeline
- Cleared FDA 510(k) K131157
- Listed FDA GUDID 00850023741202
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mc-Ran-13FA
- Generic name
- Bone access cannula
- Model / Ref / Catalog
- 13 Gauge x 5in, MC-RAN-13FA
- Primary DI / UDI-DI
- 00850023741202
- 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
- Needle Gauge — 13 GaugeLength — 5 Inch
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