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ORBIS Anesthesia

EUDAMED

Class IIa (EU MDR)

Ref ORBIS Anesthesia

by DH Healthcare GmbH

Identity

Trade Name
ORBIS Anesthesia EUDAMED
Device Name
ORBIS Anesthesia EUDAMED
Model / Reference
ORBIS Anesthesia EUDAMED

Identifiers

Primary DI / UDI-DI
04260693990019 EUDAMED
Basic UDI-DI
426069399OANESTHESIAHY EUDAMED
Direct Marketing DI
04260693990019 EUDAMED
EMDN Code
Z120499 GENERAL MEDICINE INSTRUMENTS - 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

ORBIS Anesthesia by DH Healthcare GmbH — Class IIa — 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

Manufacturer
DH Healthcare GmbH
EUDAMED SRN
DE-MF-000009069

Sources (1)

  • EUDAMED 004f3bdf-3ca1-48f0-974a-78549f517d91 61 fields · synced Jun 19, 2026