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5.0 Trocar for A-8000.23

EUDAMED

Class I (EU MDR)

Ref A-8000.24

by Medartis AG

Identity

Trade Name
5.0 Trocar for A-8000.23 EUDAMED
Device Name
Cutting & dissecting instruments EUDAMED
Model / Reference
A-8000.24 EUDAMED

Identifiers

Primary DI / UDI-DI
07630894829307 EUDAMED
Basic UDI-DI
76300378008PG EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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: Surgical retraction system, reusable

5.0 Trocar for A-8000.23 by Medartis AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Medartis AG
EUDAMED SRN
CH-MF-000022291
Authorised Representative
Medartis GmbH DE-AR-000005810

Sources (1)

  • EUDAMED c5aa72cf-8eaf-4ec2-bcf4-81ee2837e000 61 fields · synced Aug 2, 2026