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T2

by Stryker GmbH 73 variants

Ref 1830-1720SModel 08858251003290SW

T2 (1830-1720S) is a Class IIb device made by Stryker GmbH, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 08858251003290SW), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08858251003290SW Basic UDI-DI 04546540374684UDI-DIDate27 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
T2 Humerus - Anteroposterior Intramedullary Humeral Nail - Titanium Alloy - Class Iib - Sterile
Model / reference
08858251003290SW, 1830-1720S
Primary DI / UDI-DI
04546540374684
Basic UDI-DI
08858251003290SW
EMDN code
P09120201 Intramedullary nails
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
CH-MF-000009332
Authorised representative
Stryker European Operations Limited IE-AR-000000092

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Other devices filed under INTRAMEDULLARY NAILS.

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Properties

  • Supplied sterile
  • Implantable
  • Sutures
Other properties (12, all answered No)