seca 454
by seca GmbH & Co. KG 2 variants
Ref 4540000009Model ACPS001el
seca 454 (4540000009) is a Class I device made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 401203000000000000018QQ) and listed in FDA GUDID since 31 Jul 2019 (UDI-DI 04012030020091), 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 | Number401203000000000000018QQ 04012030020091 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04012030020091 | Date31 Jul 2019 | StatusListed |
Official records
- EUDAMED public site 401203000000000000018QQ
- AccessGUDID record 04012030020091
Across registries
- EUDAMED Basic UDI-DI 401203000000000000018QQ registered 5 Nov 2026 Active
- FDA GUDID UDI-DI 04012030020091 listed 31 Jul 2019 Listed
Timeline
- Listed FDA GUDID 04012030020091
- Registered EUDAMED 401203000000000000018QQ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Portable/mobile rechargeable battery pack
- Model / Ref / Catalog
- ACPS001el, 4540000009, 454
- Primary DI / UDI-DI
- 04012030020091
- Basic UDI-DI
- 401203000000000000018QQ
- Direct marketing DI
- 04012030020091
- FDA product code
- FRW
- EMDN code
- V0380 Devices with measuring functions - accessories
- GMDN term
- Portable/mobile rechargeable battery pack
- 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 | ACPS001el 4540000009 | 454 |
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