Bodymed NPP9375R
by Boxout, LLC
Bodymed NPP9375R is a Class II device made by Boxout, LLC, listed in FDA GUDID since 13 Apr 2018 (UDI-DI 00815991021688), 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 | Number00815991021688 | Date13 Apr 2018 | StatusListed |
Official records
- AccessGUDID record 00815991021688
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bodymed
- Generic name
- Transcutaneous electrical stimulation electrode, single-use
- Model / reference
- NPP9375R
- Primary DI / UDI-DI
- 00815991021688
- FDA product code
- GXY
- GMDN term
- Transcutaneous electrical stimulation electrode, single-use
- Device class
- Class II
- Regulation number
- 882.1320
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 3.75 Inch
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