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Bicontact

EUDAMED

Class IIa (EU MDR)

Ref ND830R

by Aesculap AG

Identity

Trade Name
BICONTACT EUDAMED
Device Name
BICONTACT instrument IIa EUDAMED
Model / Reference
ND830R EUDAMED

Identifiers

Primary DI / UDI-DI
04046963663261 EUDAMED
Basic UDI-DI
40392390000019463B EUDAMED
Direct Marketing DI
04046963663261 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Bicontact by Aesculap AG — Class IIa — 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 a8013694-d080-4fb5-9d84-23820c80fd22 61 fields · synced Jun 18, 2026