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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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MED PAD — 2 UDI-DI variants, MDR

MD Atlas
MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

Data from EUDAMED, last updated May 31, 2026

MED PAD

803360952MEDPAD96

2 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: 803360952MEDPAD96
Device name: MED PAD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 1, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01KBCD9JG82QP58ZV2TWWJYW48

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

MP-0108033609526611
MP-0208033609526635