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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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MEDDRAIN — 35 UDI-DI variants, MDR

MD Atlas
MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

Data from EUDAMED, last updated May 31, 2026

MEDDRAIN

803360952ACCESSORI-DRENNK

35 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: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803360952ACCESSORI-DRENNK
Device name: MEDDRAIN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL
SRN: IT-MF-000026962
Country: Italy
Email: info@medeurope.eu
Phone: +39 051810572

Variants by status

UDI-DI variants

35 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KAGV6HMRXR3CHPCJPM2FA3K4

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

TRACHEA SUCTION SET08033609527311
UV-S0208033609527120
UV-S0408033609527144
UV-N0108033609527083
CONN40X6008033609521524
CONN50M08033609527335
CONN50S08033609527588
CONN30X5008033609521517
SMH08033609522019
CONN20X4008033609521500

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