Multichem IA Pus IA321A
Part of a family of 25 devices: see the family page
Ref IA321A
Multichem IA Pus IA321A is a device classified as Class C in the EU and Class I in the US made by Techno-Path Manufacturing, registered in EUDAMED on 11 Aug 2026 (Basic UDI-DI 539152344IMMA049G) and listed in FDA GUDID since 5 Nov 2024 (UDI-DI 05391523442145), active as of 23 Oct 2026.
Active
CE IVDR
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/IVDR EUDAMED | Number539152344IMMA049G 05391523442145 | Date11 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05391523442145 | Date5 Nov 2024 | StatusListed |
Official records
- EUDAMED public site 539152344IMMA049G
- AccessGUDID record 05391523442145
Across registries
- EUDAMED Basic UDI-DI 539152344IMMA049G registered 11 Aug 2026 Active
- FDA GUDID UDI-DI 05391523442145 listed 5 Nov 2024 Listed
Timeline
- Listed FDA GUDID 05391523442145
- Registered EUDAMED 539152344IMMA049G
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Multichem IA Plus EUDAMEDMultichem IA Pus GUDID
- Generic name
- Multiple-type clinical chemistry analyte profile IVD, control
- Model / Ref / Catalog
- IA321A
- Primary DI / UDI-DI
- 05391523442145
- Basic UDI-DI
- 539152344IMMA049G
- FDA product code
- JJY
- EMDN code
- W0102152099 Controls- immunochemistry - other
- GMDN term
- Multiple-type clinical chemistry analyte profile IVD, control
- Device class
- Class C EUDAMEDClass I GUDID
- Regulation number
- 862.1660
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class C | Class I |
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