Architect 7K65-27
Ref 07K6527Model 7K65-27
Architect 7K65-27 (07K6527) is a device classified as IVD General (EU), Class I (US) made by Abbott Ireland, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00380740081126) and listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00380740081126), 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-00380740081126 00380740081126 | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00380740081126 | Date9 Sep 2016 | StatusListed |
Official records
- EUDAMED public site B-00380740081126
- AccessGUDID record 00380740081126
Across registries
- EUDAMED Basic UDI-DI B-00380740081126 registered 29 Oct 2026 Active
- FDA GUDID UDI-DI 00380740081126 listed 9 Sep 2016 Listed
Timeline
- Listed FDA GUDID 00380740081126
- Registered EUDAMED B-00380740081126
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Architect
- Generic name
- Free thyroxine (FT4) IVD, kit, chemiluminescent immunoassay
- Device name
- Free T4 (6 point calibrator assay)
- Model / Ref / Catalog
- 7K65-27, 07K6527
- Primary DI / UDI-DI
- 00380740081126
- Basic UDI-DI
- B-00380740081126
- FDA product code
- JJX, CEC, JIT
- EMDN code
- W01020401 Free triiodothyronine
- GMDN term
- Free thyroxine (FT4) IVD, kit, chemiluminescent immunoassay
- Device class
- Class IVD General EUDAMEDClass I GUDID
- Regulation number
- 862.1660, 862.1695, 862.1150
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IVD General | Class I |
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