Biotronik Scs Ndl L
Biotronik Scs Ndl L (457857) is a Class III device made by BIOTRONIK SE & Co. KG, approved under FDA PMA P210037 on 31 Mar 2023 and listed in FDA GUDID since 6 Apr 2023 (UDI-DI 04035479170288), active as of 23 Oct 2026.
Active
PMA
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04035479170288 | Date6 Apr 2023 | StatusListed |
| United States | FDA PMAAPPR | NumberP210037 | Date31 Mar 2023 | StatusActive |
Official records
- AccessGUDID record 04035479170288
- FDA PMA database P210037
Across registries
- FDA PMA P210037 decided 31 Mar 2023 Active
- FDA GUDID UDI-DI 04035479170288 listed 6 Apr 2023 Listed
Timeline
- Approved FDA PMA P210037
- Listed FDA GUDID 04035479170288
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA PMA Active
Specification
- Trade name
- Biotronik
- Generic name
- Epidural needle, non-threaded
- Model / Ref / Catalog
- SCS NDL L, 457857
- Primary DI / UDI-DI
- 04035479170288
- PMA number
- FDA product code
- LGW
- GMDN term
- Epidural needle, non-threaded
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
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