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Qolight

EUDAMED

Class IIa (EU MDR)

Ref InjeX

by Wuhan Qolight Technology Co., Ltd.

Identity

Trade Name
Qolight EUDAMED
Device Name
Vacuum Mesotherapy Device EUDAMED
Model / Reference
InjeX EUDAMED

Identifiers

Primary DI / UDI-DI
06978181510127 EUDAMED
Basic UDI-DI
697818151Q08SS EUDAMED
Direct Marketing DI
06978181510127 EUDAMED
EMDN Code
Z120611 VACUUM THERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Cupping therapy device

Qolight by Wuhan Qolight Technology Co., Ltd. — Class IIa — MDR — 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/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000046957
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED 6774d1f6-17aa-4996-9f4c-cd852ea5ab12 61 fields · synced Jun 18, 2026