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Structan

EUDAMED

Class IIa (EU MDR)

Ref NT774R

by Aesculap AG

Identity

Trade Name
STRUCTAN EUDAMED
Device Name
STRUCTAN instrument IIa EUDAMED
Model / Reference
NT774R EUDAMED

Identifiers

Primary DI / UDI-DI
04046964000584 EUDAMED
Basic UDI-DI
40392390000025382X EUDAMED
Direct Marketing DI
04046964000584 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

Yes

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

Structan 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 40778686-883c-43c9-a539-2c836dc9f93e 61 fields · synced Jun 18, 2026