Diazyme DZ112B-CAL
Ref DZ112B-CAL
Diazyme DZ112B-CAL is a device classified as IVD General made by Diazyme Laboratories, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-DZ112B-CALJJ) and listed in FDA GUDID since 3 Nov 2016 (UDI-DI D-DZ112B-CALJJ), active as of 7 Nov 2026.
Active
CE IVDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDD EUDAMED | NumberB-DZ112B-CALJJ D-DZ112B-CALJJ | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberD-DZ112B-CALJJ | Date3 Nov 2016 | StatusListed |
Official records
- EUDAMED public site B-DZ112B-CALJJ
- AccessGUDID record 00817089020184
Across registries
- EUDAMED Basic UDI-DI B-DZ112B-CALJJ registered 29 Oct 2026 Active
- FDA GUDID UDI-DI D-DZ112B-CALJJ listed 3 Nov 2016 Listed
Timeline
- Listed FDA GUDID D-DZ112B-CALJJ
- Registered EUDAMED B-DZ112B-CALJJ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Glycated Serum Protein Calibrator Set EUDAMEDDiazyme GUDID
- Generic name
- Glycated albumin IVD, calibrator
- Model / reference
- DZ112B-CAL
- Primary DI / UDI-DI
- D-DZ112B-CALJJ EUDAMED00817089020184 GUDID
- Basic UDI-DI
- B-DZ112B-CALJJ
- EMDN code
- W0101050302 Calibrators single component (cc)
- GMDN term
- Glycated albumin IVD, calibrator
- Device class
- Class IVD General
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Primary DI / UDI-DI | D-DZ112B-CALJJ | 00817089020184 |
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