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Vario

EUDAMED

Class I (EU MDR)

Ref JK758A

by Aesculap AG

Identity

Trade Name
VARIO EUDAMED
Device Name
Container EUDAMED
Model / Reference
JK758A EUDAMED

Identifiers

Primary DI / UDI-DI
04038653130795 EUDAMED
Basic UDI-DI
4039239000001151ZR EUDAMED
Direct Marketing DI
04038653130795 EUDAMED
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED

Classification

Device Class
Class I 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

Vario 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 b9c60b4a-3f88-4b79-b97f-1553e78b1230 61 fields · synced Jun 18, 2026