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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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Solutran®hemo Sistemi Accessori — 9 UDI-DI variants, MDR

MD Atlas
Meditalia Industriale Srl

Data from EUDAMED, last updated May 31, 2026

Solutran®hemo Sistemi Accessori

805848056PLTR4

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Meditalia Industriale Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805848056PLTR4
Device name: Solutran®hemo Sistemi Accessori
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Meditalia Industriale Srl
SRN: IT-MF-000032344
Country: Italy
Email: lab@meditaliasrl.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KSQA1VERN6DGGS6WPQP5AFBR

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

451100240008058480560219
451100740008058480560240
431101910008058480560196
431102010008058480560202
431100710008058480560172
431101110008058480560189
411101910008058480560158
411002000008058480560103
421102010008058480560165