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Gel Pad 15mm

EUDAMED

Class I (EU MDR)

Ref ASM000830-AA-CE

by InSightec Ltd.

Identity

Trade Name
Gel Pad 15mm EUDAMED
Device Name
Gel Pad EUDAMED
Model / Reference
ASM000830-AA-CE EUDAMED

Identifiers

Primary DI / UDI-DI
07290019402770 EUDAMED
Basic UDI-DI
7290015461GlPdSET999014GT EUDAMED
EMDN Code
Z120610 ULTRASOUND THERAPY EQUIPMENT 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

Gel Pad 15mm by Insightec Ltd — 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
InSightec Ltd.
EUDAMED SRN
IL-MF-000011795
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 1159a19e-791c-4d89-912d-bcc3bb7fe935 61 fields · synced Jul 28, 2026