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Sectra Core 26.2

by Sectra AB

Ref 101

Sectra Core 26.2 (101) is a Class IIa device made by Sectra AB, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI 735009281Archive_AppXP), 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 Number735009281Archive_AppXP Basic UDI-DI 07350092810548UDI-DIDate26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Sectra Core
Model / reference
101
Primary DI / UDI-DI
07350092810548
Basic UDI-DI
735009281Archive_AppXP
Direct marketing DI
07350092810548
EMDN code
Z110603 Picture archiving and communication systems
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000008882

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Properties

Other properties (14, all answered No)