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Bicontact S

EUDAMED

Class I (EU MDR)

Ref NT085R

by Aesculap AG

Identity

Trade Name
BICONTACT S EUDAMED
Device Name
BICONTACT instrument Ir EUDAMED
Model / Reference
NT085R EUDAMED

Identifiers

Primary DI / UDI-DI
04046963502058 EUDAMED
Basic UDI-DI
40392390000004542A EUDAMED
Direct Marketing DI
04046963502058 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS 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

Bicontact S by Aesculap AG — 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
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED be77f36c-9045-40ba-bd11-75116d104d0c 61 fields · synced Jun 18, 2026