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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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Cogel Ultrasound — 4 UDI-DI variants, MDR (COMEDICAL S.r.l.)

MD Atlas
COMEDICAL S.r.l.

Data from EUDAMED, last updated May 31, 2026

Cogel Ultrasound

805527154CUSKX

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: COMEDICAL S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805527154CUSKX
Device name: Cogel Ultrasound
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: COMEDICAL S.r.l.
SRN: IT-MF-000019319
Country: Italy
Email: info@comedical.biz
Phone: +39 0461 945876

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KR1AA60ATTAFEPJSTTSW9V89

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

CUS5000MT00208055271540054
CUS0250MF03608055271540016
CUS1000MF01208055271540030
CUS5000MS00208055271540047