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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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FREELOX RESERVE — 11 UDI-DI variants, MDR (CRYOPAL)

MD Atlas
CRYOPAL

Data from EUDAMED, last updated May 19, 2026

FREELOX RESERVE

376033557FREELOXRESERVEXA

11 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: CRYOPAL

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 376033557FREELOXRESERVEXA
Device name: —
Device model: FREELOX RESERVE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 30, 2023

Manufacturer & authorised representative

Manufacturer

Name: CRYOPAL
SRN: FR-MF-000003522
Country: France
Email: contact@cryopal.com
Phone: +33 1 64 76 15 00

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GWM91BDJ1QK44DMA7Z77VE7H

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

LF 10730103760335570346
LF10940103760335570087
LF12270103760335570117
LF10510203760335570032
LF13570003760335570148
LF10720103760335570063
LF10520103760335570056
LF13580003760335570155
LF10730003760335570070
LF13520003760335570124
LF13530003760335570131