Aneroid Kits A2-LPG
Aneroid Kits A2-LPG is a Class II device made by Rashman Corp., listed in FDA GUDID since 7 Oct 2016 (UDI-DI 00786511083984), registry data as of 23 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 | Number00786511083984 | Date7 Oct 2016 | StatusListed |
Official records
- AccessGUDID record 00786511083984
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aneroid Kits
- Generic name
- Aneroid manual sphygmomanometer
- Model / reference
- A2-LPG
- Primary DI / UDI-DI
- 00786511083984
- FDA product code
- DXQ
- GMDN term
- Aneroid manual sphygmomanometer
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- In Commercial Distribution
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