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Suction Regulator

EUDAMED

Class IIa (EU MDR)

Ref VRF-701Model VRF

by Acare Technology Co., Ltd.

Identity

Trade Name
Suction Regulator EUDAMED
Device Name
Suction Regulator EUDAMED
Model / Reference
VRF EUDAMED
VRF-701 EUDAMED

Identifiers

Primary DI / UDI-DI
04719872743040 EUDAMED
Basic UDI-DI
B-04719872743040 EUDAMED
EMDN Code
Z120611 VACUUM THERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Greece 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

Yes

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Cupping therapy device

Suction Regulator by Acare Technology Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cupping therapy device.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TW-MF-000031298
Authorised Representative
Surpass Biomedical Europe B.V. NL-AR-000038619

Sources (1)

  • EUDAMED 382639e7-3fd0-4318-96f1-ae67b7b15707 61 fields · synced Jun 20, 2026