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seca 487

by seca GmbH & Co. KG

Ref 4870045009Model ACSTI001me

seca 487 (4870045009) is a Class I device made by seca GmbH & Co. KG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 401203000000000000026QP) and listed in FDA GUDID since 7 Oct 2021 (UDI-DI 04012030021074), 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 Number401203000000000000026QP Basic UDI-DI 04012030021074UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04012030021074 UDI-DI Date7 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 401203000000000000026QP registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 04012030021074 listed 7 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04012030021074
  2. Registered EUDAMED 401203000000000000026QP

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  • Withdrawn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
Frame/rail/pole device holder
Model / Ref / Catalog
ACSTI001me, 4870045009, 487
Primary DI / UDI-DI
04012030021074
Basic UDI-DI
401203000000000000026QP
Direct marketing DI
04012030021074
FDA product code
FRI
EMDN code
V0380 Devices with measuring functions - accessories
GMDN term
Frame/rail/pole device holder
Device class
Class I
Regulation number
880.2700
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
ACSTI001me
4870045009
GUDID
487

Related devices

Category: Frame/rail/pole device holder

Similar devices in this category

Other devices filed under DEVICES WITH MEASURING FUNCTIONS - ACCESSORIES.

Other devices from seca GmbH & Co. KG

See all devices from seca GmbH & Co. KG →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)