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Covision

EUDAMED

Class I (EU MDR)

Ref 08.0840Model PARDUS INSTRUMENTS CASE

by Covision Medical Technologies Ltd.

Identity

Trade Name
COVISION EUDAMED
Device Name
PARDUS INSTRUMENTS CASE EUDAMED
Model / Reference
PARDUS INSTRUMENTS CASE EUDAMED
08.0840 EUDAMED

Identifiers

Primary DI / UDI-DI
05051659188767 EUDAMED
Basic UDI-DI
B-05051659188767 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Covision by Covision Medical Technologies Ltd. — Class I — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
GB-MF-000025081
Authorised Representative
Covision Medical Technologies (Ireland) Limited IE-AR-000031129

Sources (1)

  • EUDAMED efde6e31-0689-4ded-8a31-fd9443d751c2 61 fields · synced Oct 7, 2026