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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 — 14 UDI-DI variants, MDR (Dr. Dimitre Leonidov)

MD Atlas
Dr. Dimitre Leonidov

Data from EUDAMED, last updated May 23, 2026

cupping set

426027184LCSFB

14 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: Dr. Dimitre Leonidov

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426027184LCSFB
Device name: cupping set
Device model: LCS17
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 15, 2022

Manufacturer & authorised representative

Manufacturer

Name: Dr. Dimitre Leonidov
SRN: DE-MF-000021350
Country: Germany
Email: info@praxisbedarf-leonidov.de

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01FY66PQ9ADBH35N48B654YBCG

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

LC204260271841627
LCM204260271841863
LC0104260271841665
LCS1704260271841603
LCM104260271841856
HP104260271841580
LC504260271841658
LC304260271841634
LC104260271841610
LC404260271841641
LC004260271847247
LCS1204260271847155
HPS104260271841597
LC0204260271841672