seca 442
Ref 4420000009Model ACHR003me
seca 442 (4420000009) is a Class I device made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 401203000000000000065QZ) and listed in FDA GUDID since 7 May 2024 (UDI-DI 04012030021081), 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 | Number401203000000000000065QZ 04012030021081 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04012030021081 | Date7 May 2024 | StatusListed |
Official records
- EUDAMED public site 401203000000000000065QZ
- AccessGUDID record 04012030021081
Across registries
- EUDAMED Basic UDI-DI 401203000000000000065QZ registered 5 Nov 2026 Active
- FDA GUDID UDI-DI 04012030021081 listed 7 May 2024 Listed
Timeline
- Listed FDA GUDID 04012030021081
- Registered EUDAMED 401203000000000000065QZ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Patient height/weight-measurement standing frame
- Model / Ref / Catalog
- ACHR003me, 4420000009, 442
- Primary DI / UDI-DI
- 04012030021081
- Basic UDI-DI
- 401203000000000000065QZ
- Direct marketing DI
- 04012030021081
- FDA product code
- FRW
- EMDN code
- V0380 Devices with measuring functions - accessories
- GMDN term
- Patient height/weight-measurement standing frame
- Device class
- Class I
- Regulation number
- 880.2720
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | ACHR003me 4420000009 | 442 |
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