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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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Contone idrofilo Linea MED — 6 UDI-DI variants, MDR (IDROFIL S.R.L)

MD Atlas
IDROFIL S.R.L

Data from EUDAMED, last updated May 30, 2026

Contone idrofilo Linea MED

8020255COT00MH

6 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: IDROFIL S.R.L

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8020255COT00MH
Device name: Contone idrofilo Linea MED
Device model: Confezione da: g 1000; g 250; g 200; g 100; g 80; g 50
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 6, 2023

Manufacturer & authorised representative

Manufacturer

Name: IDROFIL S.R.L
SRN: IT-MF-000034167
Country: Italy
Email: a.carpentieri@idrofil.it

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01HC21RCDK22GE5Z9A3X4K8VQF

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

17.10108020255000008
17.10008020255000039
17.05008020255000053
17.08008020255000046
REN0108020255000114
EUROSPIN00108020255000077