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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 European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number401203000000000000007QK Basic UDI-DI 04012030020237UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04012030020237 UDI-DI Date20 Mar 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 401203000000000000007QK registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 04012030020237 listed 20 Mar 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04012030020237
  2. Registered EUDAMED 401203000000000000007QK

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

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 EUDAMED
Class 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

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
ACHR001me
4550002009
GUDID
455
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Similar devices in this category

Other devices filed under DEVICES WITH MEASURING FUNCTIONS - ACCESSORIES.

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)