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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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RETELAST — 11 UDI-DI variants, MDR (MEDINET SRL)

MD Atlas
MEDINET SRL

Data from EUDAMED, last updated May 30, 2026

RETELAST

803312340RETELASTPX

11 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: MEDINET SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803312340RETELASTPX
Device name: RETELAST
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 6, 2023

Manufacturer & authorised representative

Manufacturer

Name: MEDINET SRL
SRN: IT-MF-000011281
Country: Italy
Email: office@medinetsrl.com
Phone: +39031927288

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01H9N8N8KR4HCGDYGFR2297P43

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

RETELAST08033123400183
RETELAST08033123400077
RETELAST08033123400206
RETELAST08033123400169
RETELAST08033123400053
RETELAST08033123400138
RETELAST08033123400176
RETELAST08033123400114
RETELAST08033123400152
RETELAST08033123400091
RETELAST08033123400190