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Cupping Set

EUDAMED

Class I (EU MDR)

Ref RAB0006-2Model RAB0006Ref RAB0006-3

by RESLA GmbH

Identity

Device Name
Cupping Set EUDAMED
Model / Reference
RAB0006 EUDAMED
RAB0006-2 EUDAMED
RAB0006-3 EUDAMED

Identifiers

Primary DI / UDI-DI
08719689920593 EUDAMED
08719689920678 EUDAMED
Basic UDI-DI
8719689920RAB0006WX EUDAMED
EMDN Code
Z120611 VACUUM THERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class I 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Cupping therapy device

Cupping Set by RESLA GmbH — Class I — 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

Manufacturer
RESLA GmbH
EUDAMED SRN
DE-MF-000030425

Sources (2)

  • EUDAMED 3ee063e5-3363-4230-b7fd-db7d041a3830 61 fields · synced Jul 24, 2026
  • EUDAMED 36e8893d-b1db-4112-8f4d-537da44d686f 61 fields · synced May 18, 2026