Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

MEDDRAIN — 56 UDI-DI variants, MDR

MD Atlas
MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

Data from EUDAMED, last updated May 31, 2026

MEDDRAIN

803360952DRENAGGIUH

56 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: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803360952DRENAGGIUH
Device name: MEDDRAIN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 19, 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

56 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KAE2VW397B4P2RN1DJFZTZWJ

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

A04800790C6T08033609520923
A06401100C6T08033609521340
A06401100C6R08033609521333
A06400950C6R08033609520930
A05000700C6T08033609520299
A07901270H6S08033609521401
MED 737008033609521760
C05000700W6R08033609520251
C03350550W6R08033609520282
C06400950W6R08033609520275
C03180635W6R08033609520244
C04800790W6R08033609520268
TS5X708033609521128
TS4,8X7,908033609521104
TS6,4X11,108033609521166
TS9,5X14,308033609521241
TS3,18X6,3508033609521074
TS8X1208033609521210
TS3,35X4,6508033609521081
TS1,57x3,1808033609521036
TS2,64x4,8808033609521050
TS7X1208033609521197
TS6,4X12,708033609521173
TS1X308033609521005
TS1,02X2,1608033609521012

1 2 3