Ys-105P7
Ys-105P7 is a Class II device made by Nihon Kohden America, Inc., listed in FDA GUDID since 19 Sep 2016 (UDI-DI 00841983101939), 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 | Number00841983101939 | Date19 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00841983101939
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- General-purpose multi-parameter bedside monitor
- Model / Ref / Catalog
- YS-105P7
- Primary DI / UDI-DI
- 00841983101939
- FDA product code
- MHX
- GMDN term
- General-purpose multi-parameter bedside monitor
- Device class
- Class II
- Regulation number
- 870.1025
- GUDID distribution status
- In Commercial Distribution
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