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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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CryoFill 2.0 — 2 UDI-DI variants, MDR (Cryo Products B.V.)

MD Atlas
Cryo Products B.V.

Data from EUDAMED, last updated May 30, 2026

CryoFill 2.0

87193268205CF252

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Cryo Products B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 87193268205CF252
Device name: CryoFill 2.0
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 15, 2022

Manufacturer & authorised representative

Manufacturer

Name: Cryo Products B.V.
SRN: NL-MF-000000752
Country: Netherlands
Email: avhelvoort@cryo-products.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FTZFC563M95BAT7RCKF498VD

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

20312908719326820514
20312908719326820507