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Dornier Delta III

EUDAMED

Class IIb (EU MDR)

Ref K1044202

by Dornier MedTech GmbH

Identity

Trade Name
Dornier Delta III EUDAMED
Device Name
Dornier Delta III EUDAMED
Model / Reference
K1044202 EUDAMED

Identifiers

Primary DI / UDI-DI
D-K1044202L3 EUDAMED
Basic UDI-DI
B-K1044202L3 EUDAMED
EMDN Code
Z12020301 ELECTROMECHANICAL ENDOSCOPIC LITHOTRIPTERS 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 Delta III 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 (1)

  • EUDAMED b7f11612-c122-48c3-bdcb-9fd7616e78c2 61 fields · synced May 23, 2026