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5450040013

by Stryker Corp.

Ref 5450-040-013Model 08858250000622RT

5450040013 (5450-040-013) is a device classified as Class I in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI 08858250000622RT) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04546540716798), 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 Number08858250000622RT Basic UDI-DI 04546540716798UDI-DIDate14 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540716798 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000622RT registered 14 Sep 2026 Active
  • FDA GUDID UDI-DI 04546540716798 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04546540716798
  2. Registered EUDAMED 08858250000622RT

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  • Withdrawn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
Drilling power tool attachment, basic
Device name
S2 Drill Attachments
Model / Ref / Catalog
08858250000622RT, 5450-040-013, 5450040013
Primary DI / UDI-DI
04546540716798
Basic UDI-DI
08858250000622RT
Direct marketing DI
04546540716798
FDA product code
ERL
EMDN code
L030101 Suction and irrigation surgical cannulas and handpieces, reusable
GMDN term
Drilling power tool attachment, basic
Device class
Class I EUDAMED
Class II GUDID
Regulation number
874.4250
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 — 4.0 Centimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858250000622RT
5450-040-013
GUDID
5450040013
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: Drilling power tool attachment, basic

Similar devices

Also classified as Drilling power tool attachment, basic.

Similar devices in this category

Other devices filed under SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)