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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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textilní tejpovací náplast — 7 UDI-DI variants, MDR

MD Atlas
MEDIPLAST CZ, s.r.o.

Data from EUDAMED, last updated May 23, 2026

textilní tejpovací náplast

8595037MEDIPLASTtGK

7 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: MEDIPLAST CZ, s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8595037MEDIPLASTtGK
Device name: —
Device model: textilní tejpovací náplast
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDIPLAST CZ, s.r.o.
SRN: CZ-MF-000052351
Country: Czechia
Email: obchod@mediplast.cz
Phone: +420602162979

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPMZ1HR7S6H81MMTJ0STEE4J

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

121008595037912102
124008595037912409
1240 XTK08595037912416
122008595037912201
123008595037912300
1220 XTK08595037912218
1230 XTK08595037912317