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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 K20 Bora — 1 UDI-DI variant, MDD

MD Atlas
"KRIOMEDPOL" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Data from EUDAMED, last updated May 30, 2026

Kriopol K20 Bora

B-05905610731106

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: "KRIOMEDPOL" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

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Device characteristics

Active deviceReusable

Legacy certificates

Certificate number: DD 1023668-1
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-05905610731106
Device name: Kriopol K20 Bora
Device model: Kriopol K Bora
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Oct 17, 2023

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

basicUdiUlid01HCYM2NPR50AXXY27YH52PRWT

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