Richmar WW3005
Richmar WW3005 is a transcutaneous electrical stimulation lead (FDA Class II; FDA product code IKD, Cable, Electrode) made by Drive Devilbiss Healthcare, listed in FDA GUDID since 13 Oct 2016 (UDI-DI 00813520010240), 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 | Number00813520010240 | Date13 Oct 2016 | StatusListed |
Official records
- AccessGUDID record 00813520010240
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Richmar
- Generic name
- Transcutaneous electrical stimulation lead
- Model / reference
- WW3005
- Primary DI / UDI-DI
- 00813520010240
- FDA product code
- IKD
- GMDN term
- Transcutaneous electrical stimulation lead
- Device class
- Class II
- Regulation number
- 890.1175
- GUDID distribution status
- In Commercial Distribution
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