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Kombi Extra Stabil Beige, L M

EUDAMED

Class I (EU MDR)

Ref 7765-03

by Catell AB

Identity

Trade Name
Kombi Extra Stabil Beige, L M EUDAMED
Device Name
Combined EUDAMED
Model / Reference
7765-03 EUDAMED

Identifiers

Primary DI / UDI-DI
07340202104308 EUDAMED
Basic UDI-DI
734020217M8 EUDAMED
EMDN Code
Y060613 WRIST-HAND-FINGERS ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

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

Kombi Extra Stabil Beige, L M by Catell AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Catell AB
EUDAMED SRN
SE-MF-000000726

Sources (1)

  • EUDAMED af2cae31-014b-42d3-ba06-20d473374996 61 fields · synced Jun 18, 2026