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RenehaVis

EUDAMED

Class III (EU MDR)

Ref M311D000T

by MDT Int'l SA

Identity

Trade Name
RenehaVis EUDAMED
Device Name
RenehaVis International EUDAMED
Model / Reference
M311D000T EUDAMED

Identifiers

Primary DI / UDI-DI
07640153260048 EUDAMED
Basic UDI-DI
B-07640153260048 EUDAMED
EMDN Code
P9099 IMPLANTABLE PROSTHETIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

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

RenehaVis by MDT Int'l SA — Class III — MDD — 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

Manufacturer
MDT Int'l SA
EUDAMED SRN
CH-MF-000028146
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED f4ed0f08-dead-4dd7-b0e8-f2b3f9de301e 61 fields · synced Jul 9, 2026