Osmolarity Normal Control Solutions 100012
Ref 100012
Osmolarity Normal Control Solutions 100012 is a device classified as IVD General made by Tearlab Corporation, registered in EUDAMED on 2 Oct 2026 (Basic UDI-DI B-00853539002041) and listed in FDA GUDID since 5 Jan 2024 (UDI-DI 00853539002041), active as of 25 Oct 2026.
Active
CE IVDD
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDD EUDAMED | NumberB-00853539002041 00853539002041 | Date2 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00853539002041 | Date5 Jan 2024 | StatusListed |
Official records
- EUDAMED public site B-00853539002041
- AccessGUDID record 00853539002041
Across registries
- EUDAMED Basic UDI-DI B-00853539002041 registered 2 Oct 2026 Active
- FDA GUDID UDI-DI 00853539002041 listed 5 Jan 2024 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 00853539002041
- Registered EUDAMED B-00853539002041
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Osmolarity Control Solutions (Normal) EUDAMEDOsmolarity Normal Control Solutions GUDID
- Generic name
- Osmolality IVD, control
- Model / reference
- 100012
- Primary DI / UDI-DI
- 00853539002041
- Basic UDI-DI
- B-00853539002041
- EMDN code
- W0101050204 Electrolyte controls
- GMDN term
- Osmolality IVD, control
- Device class
- Class IVD General
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
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