Mabis 01-155-011
Mabis 01-155-011 is a Class II device made by Dms Holdings, Inc.,, cleared under FDA 510(k) K082542 on 17 Sep 2008 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00767056550117), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00767056550117 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK082542 | Date17 Sep 2008 | StatusActive |
Official records
- AccessGUDID record 00767056550117
- FDA 510(k) database K082542
Across registries
- FDA 510(k) K082542 decided 17 Sep 2008 Active
- FDA GUDID UDI-DI 00767056550117 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K082542
- Listed FDA GUDID 00767056550117
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mabis
- Generic name
- Aneroid manual sphygmomanometer
- Model / Ref / Catalog
- 01-155-011
- Primary DI / UDI-DI
- 00767056550117
- FDA product code
- DXN
- GMDN term
- Aneroid manual sphygmomanometer
- Device class
- Class II
- Regulation number
- 870.1130
- GUDID distribution status
- In Commercial Distribution
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