← Back to catalogue

Biofeedback and Stimulation System

EUDAMED

Class IIa (EU MDR)

Ref Q6

by Edan Instruments, Inc.

Identity

Trade Name
Biofeedback and Stimulation System EUDAMED
Device Name
Biofeedback and Stimulation System EUDAMED
Model / Reference
Q6 EUDAMED

Identifiers

Primary DI / UDI-DI
06944413821057 EUDAMED
Basic UDI-DI
69444138Q12SQU EUDAMED
EMDN Code
U070399 PELVIC FLOOR REHABILITATION DEVICES - OTHER 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

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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Biofeedback and Stimulation System by Edan Instruments, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

EUDAMED SRN
CN-MF-000009957
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 5fa053ed-f1d8-4e3e-926b-b8c0fbaa5fa7 61 fields · synced Jun 19, 2026