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6790-100-002

by Stryker Corp.

Ref 6790-100-002Model 08858250000668SK

6790-100-002 is a device classified as Class IIa in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 4 Jun 2026 (Basic UDI-DI 08858250000668SK) and listed in FDA GUDID since 3 Jan 2017 (UDI-DI 07613327304251), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858250000668SK Basic UDI-DI 07613327304251UDI-DIDate4 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327304251 UDI-DI Date3 Jan 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000668SK registered 4 Jun 2026 Active
  • FDA GUDID UDI-DI 07613327304251 listed 3 Jan 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327304251
  2. Registered EUDAMED 08858250000668SK

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  • Withdrawn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
Surgical irrigation tubing set, single-use
Device name
Electrosurgical Cord and Tube Sets
Model / Ref / Catalog
6790-100-002, 08858250000668SK
Primary DI / UDI-DI
07613327304251
Basic UDI-DI
08858250000668SK
FDA product code
GEI
EMDN code
K020199 Mono- and bipolar devices, single use - other
GMDN term
Surgical irrigation tubing set, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
878.4400
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

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

Related devices

Category: Surgical irrigation tubing set, single-use

Similar devices in this category

Other devices filed under MONO- AND BIPOLAR DEVICES, SINGLE USE - OTHER.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)