BioScan Gen ii
BioScan Gen ii is a Class II device made by International Health Tech, listed in FDA GUDID since 12 Aug 2026 (UDI-DI 00862719000319), 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 | Number00862719000319 | Date12 Aug 2026 | StatusListed |
Official records
- AccessGUDID record 00862719000319
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- BioScan
- Generic name
- Skin electrical conductance meter
- Model / reference
- Gen ii
- Primary DI / UDI-DI
- 00862719000319
- FDA product code
- GZO
- GMDN term
- Skin electrical conductance meter
- Device class
- Class II
- Regulation number
- 882.1540
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 8.75 InchDepth — 9.5 InchHeight — 1.5 Inch
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