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Profyle 92-23126

by Stryker Corp.

Part of a family of 48 devices: see the family page

Ref 92-23126Model 08858251003082SM

Profyle 92-23126 is a device classified as Class IIa in the EU and Class I in the US made by Stryker Corp., registered in EUDAMED on 24 Sep 2026 (Basic UDI-DI 08858251003082SM) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 07613153173731), 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 Number08858251003082SM Basic UDI-DI 07613153173731UDI-DIDate24 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613153173731 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251003082SM registered 24 Sep 2026 Active
  • FDA GUDID UDI-DI 07613153173731 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613153173731
  2. Registered EUDAMED 08858251003082SM

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  • Withdrawn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
Profyle
Generic name
Fluted surgical drill bit, single-use
Device name
Variax Instruments - Drilling Instrumentation - Class Iia - Non Sterile
Model / Ref / Catalog
92-23126, 08858251003082SM
Primary DI / UDI-DI
07613153173731
Basic UDI-DI
08858251003082SM
FDA product code
HTW
EMDN code
P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
GMDN term
Fluted surgical drill bit, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 94.0 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

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

Related devices

Category: Fluted surgical drill bit, single-use

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS - ACCESSORIES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (19, all answered No)