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Venom 0406660225

by Stryker Corp.

Part of a family of 25 devices: see the family page

Ref 0406-660-225Model 08858251003239SW

Venom 0406660225 (0406-660-225) is a device classified as Class IIa in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 16 Jul 2026 (Basic UDI-DI 08858251003239SW) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 07613327118421), 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 Number08858251003239SW Basic UDI-DI 07613327118421UDI-DIDate16 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327118421 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251003239SW registered 16 Jul 2026 Active
  • FDA GUDID UDI-DI 07613327118421 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327118421
  2. Registered EUDAMED 08858251003239SW

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  • Withdrawn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
Venom
Generic name
Percutaneous radio-frequency ablation probe cannula, single-use
Device name
RF Cannulae
Model / Ref / Catalog
08858251003239SW, 0406-660-225, 0406660225
Primary DI / UDI-DI
07613327118421
Basic UDI-DI
08858251003239SW
FDA product code
GXI
EMDN code
Z12010985 Electrosurgery instruments - consumables
GMDN term
Percutaneous radio-frequency ablation probe cannula, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
882.4725
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Length — 167.9 Millimeter
Needle Gauge — 20.0 Gauge

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858251003239SW
0406-660-225
GUDID
0406660225
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: Percutaneous radio-frequency ablation probe cannula, single-use

Similar devices in this category

Other devices filed under ELECTROSURGERY INSTRUMENTS - CONSUMABLES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)