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Medex

EUDAMED

Class I (EU MDR)

Ref 4TC1

by Medex International Inc.

Identity

Trade Name
MEDEX EUDAMED
Device Name
CHILD LAMINATION 3 ARM ANCHOR WITH ROTATION RECEIVER EUDAMED
Model / Reference
4TC1 EUDAMED

Identifiers

Primary DI / UDI-DI
00810053311516 EUDAMED
Basic UDI-DI
0810053314TC1TF EUDAMED
Direct Marketing DI
00810053311516 EUDAMED
EMDN Code
Y062499 LOWER EXTREMITY PROSTHESES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Medex by Medex International Inc. — 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

EUDAMED SRN
US-MF-000011260
Authorised Representative
Eurolink Europe Compliance Limited IE-AR-000002852

Sources (1)

  • EUDAMED 897921c2-35f0-4f74-893f-2971aabdf87d 61 fields · synced May 23, 2026