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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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GeneProof Mycoplasma genitalium/hominis… — 2 UDI-DI variants, IVDR

MD Atlas
GeneProof a.s.

Data from EUDAMED, last updated May 23, 2026

GeneProof Mycoplasma genitalium/hominis PCR Kit

859569630010Q4

2 UDI-DI variants

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

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

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 859569630010Q4
Device name: GeneProof Mycoplasma genitalium/hominis PCR Kit
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: GeneProof a.s.
SRN: CZ-MF-000002370
Country: Czechia
Email: support@geneproof.com
Phone: +420 543 211 679

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS4RX8JNRZ2S2Z2GDBRXVHQH

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

MGH/GP/10008595696300326
MGH/GP/02508595696300319