seca 455
by seca GmbH & Co. KG 2 variants
Ref 4550002009Model ACHR001me
seca 455 (4550002009) is a device classified as Class I in the EU and Class II in the US made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 401203000000000000007QK) and listed in FDA GUDID since 20 Mar 2020 (UDI-DI 04012030020237), 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 | Number401203000000000000007QK 04012030020237 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04012030020237 | Date20 Mar 2020 | StatusListed |
Official records
- EUDAMED public site 401203000000000000007QK
- AccessGUDID record 04012030020237
Across registries
- EUDAMED Basic UDI-DI 401203000000000000007QK registered 5 Nov 2026 Active
- FDA GUDID UDI-DI 04012030020237 listed 20 Mar 2020 Listed
Timeline
- Listed FDA GUDID 04012030020237
- Registered EUDAMED 401203000000000000007QK
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Patient height/weight-measurement standing frame
- Model / Ref / Catalog
- ACHR001me, 4550002009, 455
- Primary DI / UDI-DI
- 04012030020237
- Basic UDI-DI
- 401203000000000000007QK
- Direct marketing DI
- 04012030020237
- FDA product code
- PUH
- EMDN code
- V0380 Devices with measuring functions - accessories
- GMDN term
- Patient height/weight-measurement standing frame
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 870.2770
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | ACHR001me 4550002009 | 455 |
| Device class | Class I | Class II |
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