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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Cupping Set — 3 UDI-DI variants, MDR (RESLA GmbH)

MD Atlas
RESLA GmbH

Data from EUDAMED, last updated May 23, 2026

Cupping Set

8719689920RAB0006WX

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: RESLA GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8719689920RAB0006WX
Device name: Cupping Set
Device model: RAB0006
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: RESLA GmbH
SRN: DE-MF-000030425
Country: Germany
Email: alexander.lisizin@resla-gmbh.de

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GHYK1QXRREHSJDZX6K2MNC30

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

RAB0006-208719689920593
RAB0006-308719689920678
RAB0006-108719689920166