← Back to catalogue

AveCure 16G Flexible Probe

EUDAMED

Class IIb (EU MDR)

Ref 16-90-01-10

by Medwaves, Inc.

Identity

Trade Name
AveCure 16G Flexible Probe EUDAMED
Device Name
AveCure 16G Flexible Probe EUDAMED
Model / Reference
16-90-01-10 EUDAMED

Identifiers

Primary DI / UDI-DI
D-0085858400216900110NUQS EUDAMED
Basic UDI-DI
B-0085858400216900110NUQS 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 89997a9a-dc67-4fec-9b77-de12341c3626 61 fields · synced Jul 8, 2026