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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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Náplasti s polštářkem — 16 UDI-DI variants, MDR (Viacell s.r.o.)

MD Atlas
Viacell s.r.o.

Data from EUDAMED, last updated May 23, 2026

Náplasti s polštářkem

85940621400TD001W6

16 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: Viacell s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85940621400TD001W6
Device name: Náplasti s polštářkem
Device model: Náplasti s polštářkem
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Viacell s.r.o.
SRN: CZ-MF-000051827
Country: Czechia
Email: dana.kotrsova@viacell.cz

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNM1YYV0YKK2EA5M97J2MFS1

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

1986.0408594062142485
1101.04 08594062140177
1209.0408594062142614
1016.0408594062142621
1014.04 08594062140344
1042.0408594062140665
1018.0408594062140443
1041.04 08594062142232
1112.0408594062140566
1017.0408594062140481
1114.0408594062141051
1124.0408594062141037
1110.04 08594062140276
1532.04 08594062142164
1115.0408594062140696
1111.04 08594062140252