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6700-313-002

by Stryker Corp.

Ref 6700-313-002Model 08858250000641RX

6700-313-002 is a device classified as Class I in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 20 May 2026 (Basic UDI-DI 08858250000641RX) and listed in FDA GUDID since 3 Jan 2017 (UDI-DI 07613327303872), 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 Number08858250000641RX Basic UDI-DI 07613327303872UDI-DIDate20 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327303872 UDI-DI Date3 Jan 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000641RX registered 20 May 2026 Active
  • FDA GUDID UDI-DI 07613327303872 listed 3 Jan 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327303872
  2. Registered EUDAMED 08858250000641RX

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  • Withdrawn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
Foot-switch, electrical
Device name
Bipolar Generator Foot Pedal
Model / Ref / Catalog
6700-313-002, 08858250000641RX
Primary DI / UDI-DI
07613327303872
Basic UDI-DI
08858250000641RX
Direct marketing DI
07613327303872
FDA product code
GEI
EMDN code
L1899 Electrosurgery instruments, reusable - other
GMDN term
Foot-switch, electrical
Device class
Class I 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 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: Foot-switch, electrical

Similar devices in this category

Other devices filed under ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Prescription use
  • Serial number
Other properties (23, all answered No)