1352415
1352415 is a Class II device made by Medtronic Xomed Inc, listed in FDA GUDID since 15 Apr 2018 (UDI-DI 00643169938175), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00643169938175 | Date15 Apr 2018 | StatusListed |
Official records
- AccessGUDID record 00643169938175
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Transcutaneous electrical stimulation lead
- Model / reference
- 1352415
- Primary DI / UDI-DI
- 00643169938175
- FDA product code
- ETN
- GMDN term
- Transcutaneous electrical stimulation lead
- Device class
- Class II
- Regulation number
- 874.1820
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 3.0 Meter
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