← Back to catalogue

Vario

EUDAMED

Class I (EU MDR)

Ref JK369

by Aesculap AG

Identity

Trade Name
VARIO EUDAMED
Device Name
Container EUDAMED
Model / Reference
JK369 EUDAMED

Identifiers

Primary DI / UDI-DI
04038653294022 EUDAMED
Basic UDI-DI
4039239000001151ZR EUDAMED
Direct Marketing DI
04038653294022 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

Category: Instrument tray, reusable

Vario by Aesculap AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED 441574e0-8327-4879-a604-6b14718a3184 61 fields · synced Jun 19, 2026