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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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Kriopol K Bora — 1 UDI-DI variant, MDR

MD Atlas
"KRIOMEDPOL" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 30, 2026

Kriopol K Bora

590561073901D3

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: "KRIOMEDPOL" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

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Device characteristics

Active deviceReusable

Identity & classification

Basic UDI-DI: 590561073901D3
Device name: Kriopol K Bora
Device model: Kriopol K
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: "KRIOMEDPOL" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000033911
Country: Poland
Email: kriomedpol@kriomedpol.pl

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HK4VP5A5R9EKJE5B6Y1ZC59C

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

590561073110605905610731106