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MicroPro

EUDAMED

Class IIa (EU MDR)

Ref 58090010

by gbo Medizintechnik AG

Identity

Trade Name
MicroPro EUDAMED
Device Name
MicroPro EUDAMED
Model / Reference
58090010 EUDAMED

Identifiers

Primary DI / UDI-DI
04260364811230 EUDAMED
Basic UDI-DI
B-04260364811230 EUDAMED
EMDN Code
Z120608 MICROWAVE THERAPY EQUIPMENT 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

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

Category: Microwave ablation system probe, non-powered

MicroPro by Gbo Medizintechnik Ag — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system probe, non-powered.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000018065

Sources (1)

  • EUDAMED 02991162-f9b4-471d-bd41-197d6a21084c 61 fields · synced Jul 19, 2026