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T2 Alpha 2337-1232S

by Stryker Corp.

Ref 2337-1232SModel 08858251004516T8

T2 Alpha 2337-1232S is a device classified as Class IIb in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 08858251004516T8) and listed in FDA GUDID since 30 Oct 2018 (UDI-DI 07613327289299), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251004516T8 Basic UDI-DI 07613327289299UDI-DIDate27 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327289299 UDI-DI Date30 Oct 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251004516T8 registered 27 Oct 2026 Active
  • FDA GUDID UDI-DI 07613327289299 listed 30 Oct 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327289299
  2. Registered EUDAMED 08858251004516T8

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  • Withdrawn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 EUDAMED
T2 Alpha GUDID
Generic name
Femur intramedullary nail
Device name
T2 Alpha Femur Antegrade - Femoral Nail - Titanium Alloy - Class Iib - Sterile
Model / Ref / Catalog
2337-1232S, 08858251004516T8
Primary DI / UDI-DI
07613327289299
Basic UDI-DI
08858251004516T8
FDA product code
HSB
EMDN code
P09120202 Intramedullary nails in complex systems
GMDN term
Femur intramedullary nail
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
MRI safety
MR Conditional
Size
Length — 320.0 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Related devices

Category: Femur intramedullary nail

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)