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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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Sampling line (pack) — 4 UDI-DI variants, MDR (INOSYSTEMS)

MD Atlas
INOSYSTEMS

Data from EUDAMED, last updated May 19, 2026

Sampling line (pack)

376033338_INO_SAMPLINGGQ

4 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: INOSYSTEMS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376033338_INO_SAMPLINGGQ
Device name: Sampling line (pack)
Device model: Sampling line
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: INOSYSTEMS
SRN: FR-MF-000011282
Country: France
Email: contact@inosystems.fr

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JPSD6NJBXRYYRJ11G36W9BW0

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

Nebulisation filter03760333380381
Sampling flow restrictor (pack)03760333380367
Sampling line (pack)03760333380350
Water trap (pack)03760333380206