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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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Dilapan-S — 3 UDI-DI variants, MDR (MEDICEM Technology s.r.o.)

MD Atlas
MEDICEM Technology s.r.o.

Data from EUDAMED, last updated May 23, 2026

Dilapan-S

085952317DS01C3

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: MEDICEM Technology s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 085952317DS01C3
Device name: Dilapan-S
Device model: Dilapan-S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: MEDICEM Technology s.r.o.
SRN: CZ-MF-000000928
Country: Czechia
Email: technology@medicem.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GCTTHR0Y9EZWM5BEXHEV0E9X

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

DS35508595231700284
DS46508595231700260
DS45508595231700277