seca 438
Ref 4380000009Model ACMA008me
seca (4380000009) is a wheelchair-accessible platform scale (EU MDR Class I; FDA Class I; FDA product code FRW, Scale, Patient) made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 401203000000000000071QU) and listed in FDA GUDID since 1 May 2024 (UDI-DI 04012030021647), 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 | Number401203000000000000071QU 04012030021647 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04012030021647 | Date1 May 2024 | StatusListed |
Official records
- EUDAMED public site 401203000000000000071QU
- AccessGUDID record 04012030021647
Across registries
- EUDAMED Basic UDI-DI 401203000000000000071QU registered 5 Nov 2026 Active
- FDA GUDID UDI-DI 04012030021647 listed 1 May 2024 Listed
Timeline
- Listed FDA GUDID 04012030021647
- Registered EUDAMED 401203000000000000071QU
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Wheelchair-accessible platform scale
- Model / Ref / Catalog
- ACMA008me, 4380000009, 438
- Primary DI / UDI-DI
- 04012030021647
- Basic UDI-DI
- 401203000000000000071QU
- Direct marketing DI
- 04012030021647
- FDA product code
- FRW
- EMDN code
- V0380 Devices with measuring functions - accessories
- GMDN term
- Wheelchair-accessible platform scale
- 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 | ACMA008me 4380000009 | 438 |
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