Ampmed AMP1812
by Amplim, LLC
Ampmed AMP1812 is a Class II device made by Amplim, LLC, listed in FDA GUDID since 9 Jul 2019 (UDI-DI 00810477021909), 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 | Number00810477021909 | Date9 Jul 2019 | StatusListed |
Official records
- AccessGUDID record 00810477021909
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ampmed
- Generic name
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
- Model / reference
- AMP1812
- Primary DI / UDI-DI
- 00810477021909
- FDA product code
- DXN
- GMDN term
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
- Device class
- Class II
- Regulation number
- 870.1130
- GUDID distribution status
- In Commercial Distribution
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