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CryoCE AC XL+20

EUDAMED

Class IIa (EU MDR)

Ref H-AAD2100290Model Medical Family

by Auguste Cryogenics Germany GmbH

Identity

Trade Name
CryoCE AC XL+20 EUDAMED
Device Name
CryoCE AC L2 EUDAMED
Model / Reference
Medical Family EUDAMED
H-AAD2100290 EUDAMED

Identifiers

Primary DI / UDI-DI
04262416770274 EUDAMED
Basic UDI-DI
426241677MedicalFamilyCL EUDAMED
Direct Marketing DI
04262416770274 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

Category: Device sterilization/disinfection container, reusable

CryoCE AC XL+20 by Auguste Cryogenics Germany GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000019115

Sources (1)

  • EUDAMED f69babfa-076e-4d8a-8144-7c1d66eb2f93 61 fields · synced Jul 8, 2026