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APOGEPHA Ultraschallgel

EUDAMED

Class I (EU MDR)

Ref 000250735

by Göckener Gmbh

Identity

Trade Name
APOGEPHA Ultraschallgel EUDAMED
Device Name
Ultraschallgel EUDAMED
Model / Reference
000250735 EUDAMED

Identifiers

Primary DI / UDI-DI
04260746280456 EUDAMED
Basic UDI-DI
426074628362 EUDAMED
Direct Marketing DI
04260746280456 EUDAMED
EMDN Code
Z11040185 ULTRASOUND SCANNERS - CONSUMABLES EUDAMED

Classification

Device Class
Class I 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

APOGEPHA Ultraschallgel by Göckener Gmbh — Class I — 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
Göckener Gmbh
EUDAMED SRN
DE-MF-000009282

Sources (1)

  • EUDAMED e0b89a60-2162-44bd-9240-472f64b61c1b 61 fields · synced Jul 31, 2026