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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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Gomedic 2D — 1 UDI-DI variant, MDR (Sensor Medica Srl)

MD Atlas
Sensor Medica Srl

Data from EUDAMED, last updated May 31, 2026

Gomedic 2D

8052015181047TC

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Sensor Medica Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8052015181047TC
Device name: Gomedic 2D
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: Sensor Medica Srl
SRN: IT-MF-000032343
Country: Italy
Email: info@sensormedica.com
Phone: +390640061200

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KKY5VWHNPF3CTCZGTB07HPJD

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

Gomedic 2D08052015181047