Locator™ 1281-58
Locator™ 1281-58 is a Class III device made by St. Jude Medical, Inc., approved under FDA PMA P960013 on 20 Jun 1997 and listed in FDA GUDID since 6 Feb 2017 (UDI-DI 05414734501125), 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 | Number05414734501125 | Date6 Feb 2017 | StatusListed |
| United States | FDA PMAAPPR | NumberP960013 | Date20 Jun 1997 | StatusActive |
Official records
- AccessGUDID record 05414734501125
- FDA PMA database P960013
Across registries
- FDA PMA P960013 decided 20 Jun 1997 Active
- FDA GUDID UDI-DI 05414734501125 listed 6 Feb 2017 Listed
Timeline
- Approved FDA PMA P960013
- Listed FDA GUDID 05414734501125
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA PMA Active
Specification
- Trade name
- Locator™
- Generic name
- Pacing/defibrillation lead stylet
- Model / Ref / Catalog
- 1281-58
- Primary DI / UDI-DI
- 05414734501125
- PMA number
- FDA product code
- NVZ
- GMDN term
- Pacing/defibrillation lead stylet
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 58 Centimeter
Similar devices in this category
Other devices filed under Pacing/defibrillation lead stylet.