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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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Petriho miska Ø 90 mm AP — 7 UDI-DI variants, IVDR (GAMA GROUP a.s.)

MD Atlas
GAMA GROUP a.s.

Data from EUDAMED, last updated May 23, 2026

Petriho miska Ø 90 mm AP

85935402PETRIHOMISKYR4

7 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: GAMA GROUP a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85935402PETRIHOMISKYR4
Device name: Petriho miska Ø 90 mm AP
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 27, 2022

Manufacturer & authorised representative

Manufacturer

Name: GAMA GROUP a.s.
SRN: CZ-MF-000011894
Country: Czechia
Email: gama.jim@gama.cz

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01G6304MS8T07ZHW7C4FT48N3G

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

Petri dish Ø 90 mm AP - EN08593540354181
Petri dish Ø 90 mm AP 2-compartment - EN08593540354242
Petri dish Ø 90 mm AP 3-compartment - EN08593540354273
V20442008593540354082
V20442108593540354129
V20442208593540354150
V204420-PL08593540354211