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Dornier Aries 2

EUDAMED

Class IIb (EU MDR)

Ref K1042826Ref K1040131Ref K1042827

by Dornier MedTech GmbH

Identity

Trade Name
Dornier Aries 2 EUDAMED
Device Name
Dornier Aries 2 EUDAMED
Model / Reference
K1042826 EUDAMED
K1040131 EUDAMED
K1042827 EUDAMED

Identifiers

Primary DI / UDI-DI
04049957005900 EUDAMED
04049957005313 EUDAMED
04049957005917 EUDAMED
Basic UDI-DI
B-04049957005900 EUDAMED
B-04049957005313 EUDAMED
B-04049957005917 EUDAMED
EMDN Code
Z12139001 SHOCK WAVE THERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Dornier Aries 2 by Dornier Medtech Gmbh — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000009774

Sources (3)

  • EUDAMED 4a5e7268-285f-4746-bde1-06bec7146248 61 fields · synced Aug 4, 2026
  • EUDAMED 3adee779-d5c8-451a-bd48-c518f184be26 61 fields · synced May 18, 2026
  • EUDAMED 1af177b1-aa44-4234-ac14-768661508541 61 fields · synced May 19, 2026