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Dornier Delta III Pro

EUDAMED

Class IIb (EU MDR)

Ref K1045936

by Dornier MedTech GmbH

Identity

Trade Name
Dornier Delta III Pro EUDAMED
Device Name
Dornier Delta III EUDAMED
Model / Reference
K1045936 EUDAMED

Identifiers

Primary DI / UDI-DI
04049957006457 EUDAMED
Basic UDI-DI
4049957DornierDeltaIIIF5 EUDAMED
EMDN Code
Z12160101 EXTRACORPOREAL 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

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

Dornier Delta III Pro by Dornier Medtech Gmbh — Class IIb — 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

EUDAMED SRN
DE-MF-000009774

Sources (1)

  • EUDAMED 28220c2c-f72f-416a-82ec-7ffdb16854ad 61 fields · synced Jun 18, 2026