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seca 201

by seca GmbH & Co. KG 2 variants

Ref 2011817009Model MDCMS001memf

seca (2011817009) is a patient-height measure (EU MDD 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 B-04012030007269) and listed in FDA GUDID since 1 Oct 2024 (UDI-DI 04012030007269), active as of 12 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

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/MDD EUDAMED NumberB-04012030007269 Basic UDI-DI 04012030007269UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04012030007269 UDI-DI Date1 Oct 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04012030007269 registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 04012030007269 listed 1 Oct 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04012030007269
  2. Registered EUDAMED B-04012030007269

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Generic name
Patient-height measure
Model / Ref / Catalog
MDCMS001memf, 2011817009, 201
Primary DI / UDI-DI
04012030007269
Basic UDI-DI
B-04012030007269
Direct marketing DI
04012030007269
FDA product code
FRW
EMDN code
V0399 Measurement devices - other
GMDN term
Patient-height measure
Device class
Class I
Regulation number
880.2720
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MDCMS001memf
2011817009
GUDID
201

Related devices

Category: Patient-height measure

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Other devices filed under MEASUREMENT DEVICES - OTHER.

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Properties

  • Premarket exempt
  • Lot / batch number
Other properties (23, all answered No)