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Trendhip

EUDAMED

Class IIa (EU MDR)

Ref NF322R

by Aesculap AG

Identity

Trade Name
TRENDHIP EUDAMED
Device Name
TRENDHIP instrument EUDAMED
Model / Reference
NF322R EUDAMED

Identifiers

Primary DI / UDI-DI
04046964219870 EUDAMED
Basic UDI-DI
403923900000285136 EUDAMED
Direct Marketing DI
04046964219870 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

Trendhip 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 cc39f967-f49d-412e-b0c6-1ec7e816069b 61 fields · synced Jun 18, 2026