seca 477
Ref 4770000009Model ACHR002me
seca 477 (4770000009) is a Class I device made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 401203000000000000023QH) and listed in FDA GUDID since 8 Sep 2020 (UDI-DI 04012030020725), active as of 12 Nov 2026.
Active
CE MDR
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/MDR EUDAMED | Number401203000000000000023QH 04012030020725 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04012030020725 | Date8 Sep 2020 | StatusListed |
Official records
- EUDAMED public site 401203000000000000023QH
- AccessGUDID record 04012030020725
Across registries
- EUDAMED Basic UDI-DI 401203000000000000023QH registered 5 Nov 2026 Active
- FDA GUDID UDI-DI 04012030020725 listed 8 Sep 2020 Listed
Timeline
- Listed FDA GUDID 04012030020725
- Registered EUDAMED 401203000000000000023QH
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Patient height/weight-measurement standing frame
- Model / Ref / Catalog
- ACHR002me, 4770000009, 477
- Primary DI / UDI-DI
- 04012030020725
- Basic UDI-DI
- 401203000000000000023QH
- Direct marketing DI
- 04012030020725
- FDA product code
- FRI
- EMDN code
- V0380 Devices with measuring functions - accessories
- GMDN term
- Patient height/weight-measurement standing frame
- Device class
- Class I
- Regulation number
- 880.2700
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | ACHR002me 4770000009 | 477 |
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