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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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PLATINO — 308 UDI-DI variants, MDR (INVE.COMM. Srl )

MD Atlas
INVE.COMM. Srl

Data from EUDAMED, last updated May 31, 2026

PLATINO

805612187MAT66AB22EMXM

308 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: INVE.COMM. Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805612187MAT66AB22EMXM
Device name: PLATINO
Device model: MATERASSO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: INVE.COMM. Srl
SRN: IT-MF-000055002
Country: Italy
Email: amministrazione@invecomm.com
Phone: +390688588126

Variants by status

UDI-DI variants

308 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7XX1R2SQYDAED63JBTPCRT

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

0006708056121874534
0006708056121874473
0006708056121874435
0006708056121874510
0006708056121874411
0006708056121874404
0006708056121874480
0001808056121875814