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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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gb PHARM DPYD — 2 UDI-DI variants, IVDR (GENERI BIOTECH s.r.o.)

MD Atlas
GENERI BIOTECH s.r.o.

Data from EUDAMED, last updated May 23, 2026

gb PHARM DPYD

85952239000020WY

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: GENERI BIOTECH s.r.o.

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Device characteristics

Professional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 85952239000020WY
Device name: gb PHARM DPYD
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Oct 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: GENERI BIOTECH s.r.o.
SRN: CZ-MF-000018857
Country: Czechia
Email: info@generi-biotech.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HCM6WKFNCQYHGVYCTSMYETNP

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

3255-05008595223925527
3255-02508595223925510