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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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FILMPORE /FILMPORE — 3 UDI-DI variants, MDR (BATIST Medical a.s.)

MD Atlas
BATIST Medical a.s.

Data from EUDAMED, last updated May 23, 2026

FILMPORE /FILMPORE

8591454doc009MH

3 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: 8591454doc009MH
Device name: FILMPORE /FILMPORE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 14, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KP629P0WJQ6G663FGNKBC70K

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

FILMPORE PE Transparent Tape 1,25cmx9,15m08591454003294
FILMPORE PE Transparent Tape 2,5cmx9,15m08591454003317
FILMPORE PE Transparent Tape 5cmx9,15m08591454003331