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T2 1822-0010S

by Stryker Corp.

Ref 1822-0010SModel 08858251004545TF

T2 1822-0010S is a device classified as Class IIb in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 7 Oct 2026 (Basic UDI-DI 08858251004545TF) and listed in FDA GUDID since 24 Sep 2015 (UDI-DI 04546540197566), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251004545TF Basic UDI-DI 04546540197566UDI-DIDate7 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540197566 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251004545TF registered 7 Oct 2026 Active
  • FDA GUDID UDI-DI 04546540197566 listed 24 Sep 2015 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04546540197566
  2. Registered EUDAMED 08858251004545TF

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  • Withdrawn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
Bone nail implantable cap
Device name
T2 Screws + End Caps - End Cap - Titanium Alloy - Class Iib - Sterile
Model / Ref / Catalog
1822-0010S, 08858251004545TF
Primary DI / UDI-DI
04546540197566
Basic UDI-DI
08858251004545TF
FDA product code
HSB
EMDN code
P09120299 Osteosynthesis nails - other
GMDN term
Bone nail implantable cap
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

Related devices

Category: Bone nail end-cap

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)