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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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LINICIN FLASH — 5 UDI-DI variants, MDR

MD Atlas
Coopération pharmaceutique française

Data from EUDAMED, last updated May 19, 2026

LINICIN FLASH

37015101008222

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: Coopération pharmaceutique française

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37015101008222
Device name: LINICIN FLASH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Coopération pharmaceutique française
SRN: FR-MF-000002412
Country: France
Email: info.med@cooperconsumerhealth.com
Phone: +33 1 64 87 20 00

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KJW11JBDNTWB65YM0XN4GJVF

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

AFT40055045803701510101726
AFT40055045903701510101733
POUXIT FLASH 150mL03701510101757
POUXIT FLASH 150mL LOT 203701510101764
POUXIT FLASH 200mL03701510101740