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AveCure 16G Flexible Probe

EUDAMED

Class IIb (EU MDR)

Ref 16-123-01-15

by Medwaves, Inc.

Identity

Trade Name
AveCure 16G Flexible Probe EUDAMED
Device Name
AveCure 16G Flexible Probe EUDAMED
Model / Reference
16-123-01-15 EUDAMED

Identifiers

Primary DI / UDI-DI
D-0858584002161230115UKWP EUDAMED
Basic UDI-DI
B-0858584002161230115UKWP EUDAMED
EMDN Code
K02030199 RADIOFREQUENCY SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

AveCure 16G Flexible Probe by Medwaves, Inc. — Class IIb — 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

Manufacturer
Medwaves, Inc.
EUDAMED SRN
US-MF-000053179
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 364a7fe5-5b00-4ec7-81de-bd478423fca6 61 fields · synced Jun 18, 2026