Architect 2K48-01
Ref 02K4801Model 2K48-01
Architect 2K48-01 (02K4801) is a device classified as IVD General (EU), Class I (US) made by Abbott Laboratories, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00380740003494) and listed in FDA GUDID since 6 Jun 2016 (UDI-DI 00380740003494), 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-00380740003494 00380740003494 | Date30 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00380740003494 | Date6 Jun 2016 | StatusListed |
Official records
- EUDAMED public site B-00380740003494
- AccessGUDID record 00380740003494
Across registries
- EUDAMED Basic UDI-DI B-00380740003494 registered 30 Oct 2026 Active
- FDA GUDID UDI-DI 00380740003494 listed 6 Jun 2016 Listed
Timeline
- Listed FDA GUDID 00380740003494
- Registered EUDAMED B-00380740003494
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Architect
- Generic name
- Multiple thyroid hormone uptake (T-uptake) IVD, calibrator
- Device name
- T-Uptake
- Model / Ref / Catalog
- 2K48-01, 02K4801
- Primary DI / UDI-DI
- 00380740003494
- Basic UDI-DI
- B-00380740003494
- FDA product code
- JJX, JIT
- EMDN code
- W0102152208 Standards and calibrators for individual and specific hormones /proteins
- GMDN term
- Multiple thyroid hormone uptake (T-uptake) IVD, calibrator
- Device class
- Class IVD General EUDAMEDClass I GUDID
- Regulation number
- 862.1660, 862.1150
- 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 |
|---|---|---|
| Device class | Class IVD General | Class I |
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