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Occlutech Delivery Set

EUDAMED

Class III (EU MDR)

Ref 51US007Ref 51US006Ref 51DS010

by Occlutech GmbH

Identity

Trade Name
Occlutech Delivery Set EUDAMED
Device Name
Occlutech Delivery Set EUDAMED
Model / Reference
51US007 EUDAMED
51US006 EUDAMED
51DS010 EUDAMED

Identifiers

Primary DI / UDI-DI
04260182521816 EUDAMED
04260182521809 EUDAMED
04260182521762 EUDAMED
Basic UDI-DI
426018252ODSI7T EUDAMED
EMDN Code
C0502 CARDIOVASCULAR INTRODUCER SHEATHS, VALVED EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Vascular catheter introduction set, nonimplantable

Occlutech Delivery Set by Occlutech GmbH — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Occlutech GmbH
EUDAMED SRN
DE-MF-000005104

Sources (3)

  • EUDAMED 0688bc9e-8fdd-4653-bfcf-3667adf0cf17 61 fields · synced Oct 1, 2026
  • EUDAMED 5a63ca41-ca99-41df-9bfb-80c6543ae844 61 fields · synced May 17, 2026
  • EUDAMED e390512d-60aa-4730-abdf-61a1e63636d0 61 fields · synced May 17, 2026