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Aptus Tourguide

by Oscor Inc. 10 variants

Ref TG0655517

Aptus Tourguide (TG0655517) is a Class III device made by Oscor Inc., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00885672012243), active as of 7 Nov 2026.

Active European Union

CE MDD

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/MDD NumberB-00885672012243 Basic UDI-DI 00885672012243UDI-DIDate30 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
TG0655517
Primary DI / UDI-DI
00885672012243
Basic UDI-DI
B-00885672012243
EMDN code
C0599 Cardiovascular introducer sheaths - other
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000005944
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under CARDIOVASCULAR INTRODUCER SHEATHS - OTHER.

Other devices from Oscor Inc.

See all devices from Oscor Inc. →

Properties

  • Supplied sterile
Other properties (13, all answered No)