Skip to content

T2 1818-0001S

by Stryker Corp.

Ref 1818-0001SModel 08858251004495TR

T2 1818-0001S is a device classified as Class IIb in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 12 Oct 2026 (Basic UDI-DI 08858251004495TR) and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 04546540673213), 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 Number08858251004495TR Basic UDI-DI 04546540673213UDI-DIDate12 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540673213 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251004495TR registered 12 Oct 2026 Active
  • FDA GUDID UDI-DI 04546540673213 listed 24 Sep 2015 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04546540673213
  2. Registered EUDAMED 08858251004495TR

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  • Withdrawn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
T2
Generic name
Orthopaedic bone screw (non-sliding)
Device name
T2 Ankle - Compression Screw - Titanium Alloy - Class Iib - Sterile
Model / Ref / Catalog
1818-0001S, 08858251004495TR
Primary DI / UDI-DI
04546540673213
Basic UDI-DI
08858251004495TR
FDA product code
HSB
EMDN code
P09120604 Osteosynthesis nail-screw systems
GMDN term
Orthopaedic bone screw (non-sliding)
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3020
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 IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb 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: Orthopaedic bone screw (non-sliding)

Similar devices in this category

Other devices filed under BONE FIXATION SCREWS, TENDON AND LIGAMENT SYNTHESIS SCREWS.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Sutures
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)