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0682400605

by STRYKER Communications, Inc.

Ref 0682-400-605Model 08858250000752S9

0682400605 (0682-400-605) is a Class I device made by STRYKER Communications, Inc., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 08858250000752S9) and listed in FDA GUDID since 29 Jul 2020 (UDI-DI 07613327054521), active as of 7 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858250000752S9 Basic UDI-DI 07613327054521UDI-DIDate4 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327054521 UDI-DI Date29 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000752S9 registered 4 Nov 2026 Active
  • FDA GUDID UDI-DI 07613327054521 listed 29 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327054521
  2. Registered EUDAMED 08858250000752S9

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  • Withdrawn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
Medical monitor/light mount
Device name
COM_TF10468_Suspension
Model / Ref / Catalog
08858250000752S9, 0682-400-605, 0682400605
Primary DI / UDI-DI
07613327054521
Basic UDI-DI
08858250000752S9
Direct marketing DI
07613327054521
FDA product code
FQO
EMDN code
Z129099 Various instruments for functional exploration and therapeutic interventions - other
GMDN term
Medical monitor/light mount
Device class
Class I
Regulation number
878.4960
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858250000752S9
0682-400-605
GUDID
0682400605

Related devices

Category: Medical monitor/light mount

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - OTHER.

Other devices from STRYKER Communications, Inc.

See all devices from STRYKER Communications, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (22, all answered No)