Immunalysis 10009-15
Ref 10009-15
Immunalysis 10009-15 is an opiate/opiate metabolite IVD (EU IVDD general IVD; FDA Class I; FDA product code DIF, Drug mixture control materials) made by Immunalysis Corporation, registered in EUDAMED on 31 Aug 2026 (Basic UDI-DI B-00840937108307) and listed in FDA GUDID since 13 Sep 2016 (UDI-DI 00840937108307), active as of 23 Oct 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-00840937108307 00840937108307 | Date31 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00840937108307 | Date13 Sep 2016 | StatusListed |
Official records
- EUDAMED public site B-00840937108307
- AccessGUDID record 00840937108307
Across registries
- EUDAMED Basic UDI-DI B-00840937108307 registered 31 Aug 2026 Active
- FDA GUDID UDI-DI 00840937108307 listed 13 Sep 2016 Listed
Timeline
- Listed FDA GUDID 00840937108307
- Registered EUDAMED B-00840937108307
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Immunalysis
- Generic name
- Opiate/opiate metabolite IVD, calibrator
- Model / Ref / Catalog
- 10009-15
- Primary DI / UDI-DI
- 00840937108307
- Basic UDI-DI
- B-00840937108307
- FDA product code
- DIF
- EMDN code
- W0102152209 Drugs of abuse / toxicology standards and calibrators
- GMDN term
- Opiate/opiate metabolite IVD, calibrator
- Device class
- Class IVD General EUDAMEDClass I GUDID
- Regulation number
- 862.3280
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IVD General | Class I |
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