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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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Liflow — 2 UDI-DI variants, MDR (INTRASENSE)

MD Atlas
INTRASENSE

Data from EUDAMED, last updated May 19, 2026

Liflow

37007197LiflowAQ

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: INTRASENSE

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 37007197LiflowAQ
Device name: Liflow
Device model: Liflow
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Nov 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: INTRASENSE
SRN: FR-MF-000001551
Country: France
Email: contact@intrasense.fr
Phone: +334 67 13 01 35

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HW4Y4KEK83TS6V1KN6CECW81

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

Liflow 2.003700719700709
Liflow® 3.003700719701096