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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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Traverse Monouso — 2 UDI-DI variants, MDR (IDROFIL S.R.L)

MD Atlas
IDROFIL S.R.L

Data from EUDAMED, last updated May 31, 2026

Traverse Monouso

8020255TRAVERSE057J

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: IDROFIL S.R.L

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UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQ758F585QM9MNT1KJQDX5EH

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

05.00508020255000138
05.00408020255000121

Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 8020255TRAVERSE057J
Device name: Traverse Monouso
Device model: Traverse Monouso non rimboccabili
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

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

Variants by status