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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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Personal lubricant water-based without… — 2 UDI-DI variants, MDR

MD Atlas
Cosmonde, a.s.

Data from EUDAMED, last updated May 23, 2026

Personal lubricant water-based without flavour

85950039CM001HZ

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Cosmonde, a.s.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2025-MDR/QS-029/A
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Feb 10, 2026 → May 13, 2030

Identity & classification

Basic UDI-DI: 85950039CM001HZ
Device name: Personal lubricant water-based without flavour
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Cosmonde, a.s.
SRN: CZ-MF-000029535
Country: Czechia
Email: info@cosmonde.cz
Phone: +420 516 770 000

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KK1MY0V8EEZFAPRAGFJ4CK1X

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

Z100108595003904148
Z100008595003904155