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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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VAROPAD GENITAAL MAN — 3 UDI-DI variants, MDR

MD Atlas
Softcompress Dennis Ptasik

Data from EUDAMED, last updated May 30, 2026

VAROPAD GENITAAL MAN

426258979040FE

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: Softcompress Dennis Ptasik

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426258979040FE
Device name: —
Device model: VAROPAD GENITAAL MAN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Softcompress Dennis Ptasik
SRN: DE-MF-000025752
Country: Germany
Email: info@softcompress.de
Phone: 02015139242

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSMJZZBY09QP4G6NS2SW5Z31

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

V840-104262589793209
V840-204262589793216
V840-304262589793223