seca 403
Ref 4030000009Model ACBAS001me
seca 403 (4030000009) is a Class I device made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 401203000000000000014QG) and listed in FDA GUDID since 13 May 2022 (UDI-DI 04012030014540), 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 | Number401203000000000000014QG 04012030014540 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04012030014540 | Date13 May 2022 | StatusListed |
Official records
- EUDAMED public site 401203000000000000014QG
- AccessGUDID record 04012030014540
Across registries
- EUDAMED Basic UDI-DI 401203000000000000014QG registered 5 Nov 2026 Active
- FDA GUDID UDI-DI 04012030014540 listed 13 May 2022 Listed
Timeline
- Listed FDA GUDID 04012030014540
- Registered EUDAMED 401203000000000000014QG
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Electromechanical device/system transport trolley
- Model / Ref / Catalog
- ACBAS001me, 4030000009, 403
- Primary DI / UDI-DI
- 04012030014540
- Basic UDI-DI
- 401203000000000000014QG
- Direct marketing DI
- 04012030014540
- FDA product code
- FRW
- EMDN code
- V0380 Devices with measuring functions - accessories
- GMDN term
- Electromechanical device/system transport trolley
- Device class
- Class I
- Regulation number
- 880.2720
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | ACBAS001me 4030000009 | 403 |
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