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Multigen 2 8400-800-000

by Stryker Corp.

Ref 8400-800-000Model 08858250000009R5

Multigen 2 8400-800-000 is an electrosurgical cable adaptor (EU MDR Class I; FDA Class II; FDA product code GXD, Generator, Lesion, Radiofrequency) made by Stryker Corp., registered in EUDAMED on 24 Jun 2026 (Basic UDI-DI 08858250000009R5) and listed in FDA GUDID since 15 Jun 2017 (UDI-DI 07613327173666), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858250000009R5 Basic UDI-DI 07613327173666UDI-DIDate24 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327173666 UDI-DI Date15 Jun 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000009R5 registered 24 Jun 2026 Active
  • FDA GUDID UDI-DI 07613327173666 listed 15 Jun 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327173666
  2. Registered EUDAMED 08858250000009R5

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  • Withdrawn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

Trade name
Multigen 2
Generic name
Electrosurgical cable adaptor
Device name
RF Cables
Model / Ref / Catalog
8400-800-000, 08858250000009R5
Primary DI / UDI-DI
07613327173666
Basic UDI-DI
08858250000009R5
Direct marketing DI
07613327173666
FDA product code
GXD
EMDN code
Z12010980 Electrosurgery instruments - hardware accessories
GMDN term
Electrosurgical cable adaptor
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.4400
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 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.

Related devices

Category: Electrosurgical cable adaptor

Similar devices in this category

Other devices filed under ELECTROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)