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Bipolar Wand

EUDAMED

Class IIb (EU MDR)

Ref SDTFQM-40

by Soniquence, LLC

Identity

Trade Name
Bipolar Wand EUDAMED
Device Name
Bipolar Wand EUDAMED
Model / Reference
SDTFQM-40 EUDAMED

Identifiers

Primary DI / UDI-DI
00810026182419 EUDAMED
Basic UDI-DI
0081002618SDTFQM-40TQ EUDAMED
EMDN Code
K0201010301 OPEN ELECTROSURGERY ELECTRODES, SINGLE-USE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

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

Bipolar Wand by Soniquence, LLC — Class IIb — 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
Soniquence, LLC
EUDAMED SRN
US-MF-000029810
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 91bc885e-4168-40e4-b93a-f16e9e88d809 61 fields · synced May 22, 2026