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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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NESTERILNÍ NÁPLASTI / NON-STERILE… — 7 UDI-DI variants, MDR

MD Atlas
BATIST Medical a.s.

Data from EUDAMED, last updated May 23, 2026

NESTERILNÍ NÁPLASTI / NON-STERILE PLASTERS

8591454doc008MF

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: BATIST Medical a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591454doc008MF
Device name: NESTERILNÍ NÁPLASTI / NON-STERILE PLASTERS
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: BATIST Medical a.s.
SRN: CZ-MF-000023038
Country: Czechia
Email: batist@batist.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNKZZ4YFN7GY0ABN6QE9ZS69

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

ELASTPORE Nonwoven Plaster in Roll 10cmx10m08591454013873
ELASTPORE Nonwoven Plaster in Roll 15cmx10m08591454013866
ELASTPORE Nonwoven Plaster in Roll 20cmx10m08591454013859
ELASTPORE Nonwoven Plaster in Roll 5cmx10m08591454013897
SOFTPORE Non woven Tape 1,25cmx9,15m08591454003171
SOFTPORE Non woven Tape 2,5cmx9,15m08591454003195
SOFTPORE Non woven Tape 5cmx9,15m08591454003218