Pro Clean 9011992
by Premier Dental Products Company
Ref 9011992
Pro Clean 9011992 is a Class I device made by Premier Dental Products Company, registered in EUDAMED on 5 Jun 2026 (Basic UDI-DI 00348783ProCleanAK) and listed in FDA GUDID since 29 Jun 2022 (UDI-DI 00348783003840), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number00348783ProCleanAK 00348783003840 | Date5 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00348783003840 | Date29 Jun 2022 | StatusListed |
Official records
- EUDAMED public site 00348783ProCleanAK
- AccessGUDID record 00348783003840
Across registries
- EUDAMED Basic UDI-DI 00348783ProCleanAK registered 5 Jun 2026 Active
- FDA GUDID UDI-DI 00348783003840 listed 29 Jun 2022 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 00348783003840
- Registered EUDAMED 00348783ProCleanAK
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- PRO CLEAN SAMPLE (1pk) EUDAMEDPro Clean GUDID
- Generic name
- Denture cleanser
- Model / reference
- 9011992
- Primary DI / UDI-DI
- 00348783003840
- Basic UDI-DI
- 00348783ProCleanAK
- FDA product code
- JER
- EMDN code
- D0899 Detergents for medical devices - other
- GMDN term
- Denture cleanser
- Device class
- Class I
- Regulation number
- 872.3530
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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