Smartmagnet™ 9322
Smartmagnet™ 9322 is a Class III device made by Medtronic, Inc., listed in FDA GUDID since 23 Sep 2014 (UDI-DI 00681490197885), registry data as of 22 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 | Number00681490197885 | Date23 Sep 2014 | StatusListed |
Official records
- AccessGUDID record 00681490197885
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Smartmagnet™
- Generic name
- Cardiac pulse generator test magnet
- Model / reference
- 9322
- Primary DI / UDI-DI
- 00681490197885
- FDA product code
- LWS, NIK
- GMDN term
- Cardiac pulse generator test magnet
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
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