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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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Kit Double Sachet — 5 UDI-DI variants, MDR (Verreries Talançonnaises)

MD Atlas
Verreries Talançonnaises

Data from EUDAMED, last updated May 19, 2026

Kit Double Sachet

0376039695-Cryokit-DS-RP

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Verreries Talançonnaises

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0376039695-Cryokit-DS-RP
Device name: Kit Double Sachet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Verreries Talançonnaises
SRN: FR-MF-000019313
Country: France
Email: qualite@flacons-vt.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KE9DYY76CXAVR6N1T9EBG87E

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

38250021F03760396950064
3825002103760396950033
38250021B03760396950040
3825002203760396950057
382500203760396950026