Architect 7K66-32
Part of a family of 9 devices: see the family page
Ref 07K6632
Architect 7K66-32 (07K6632) is a device classified as Class B in the EU and Class II in the US made by Abbott Ireland, registered in EUDAMED on 19 Aug 2026 (Basic UDI-DI 038074ARK0766NL) and listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00380740129491), 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 | Number038074ARK0766NL 00380740129491 | Date19 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00380740129491 | Date9 Sep 2016 | StatusListed |
Official records
- EUDAMED public site 038074ARK0766NL
- AccessGUDID record 00380740129491
Across registries
- EUDAMED Basic UDI-DI 038074ARK0766NL registered 19 Aug 2026 Active
- FDA GUDID UDI-DI 00380740129491 listed 9 Sep 2016 Listed
Timeline
- Listed FDA GUDID 00380740129491
- Registered EUDAMED 038074ARK0766NL
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Architect
- Generic name
- Total thyroxine (TT4) IVD, kit, chemiluminescent immunoassay
- Device name
- ARCHITECT Total T4
- Model / Ref / Catalog
- 07K6632, 7K66-32
- Primary DI / UDI-DI
- 00380740129491
- Basic UDI-DI
- 038074ARK0766NL
- FDA product code
- JIT, KLI, JJX
- EMDN code
- W01020407 Thyroxine
- GMDN term
- Total thyroxine (TT4) IVD, kit, chemiluminescent immunoassay
- Device class
- Class B EUDAMEDClass II GUDID
- Regulation number
- 862.1150, 862.1700, 862.1660
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 07K6632 | 7K66-32 |
| Device class | Class B | Class II |
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