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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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Holos Global System — 40 UDI-DI variants, MDR (Key4Product srl)

MD Atlas
Key4Product srl

Data from EUDAMED, last updated May 30, 2026

Holos Global System

805758765Holos5P

40 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: Key4Product srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805758765Holos5P
Device name: Holos Global System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: Key4Product srl
SRN: IT-MF-000035891
Country: Italy
Email: domenico.lioy@key4product.com
Phone: +393468532308

Variants by status

UDI-DI variants

40 UDI-DI variants

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Applied filters

basicUdiUlid01H5SPVW7ZFBBVH51F9VDGN6CY

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

MIO-4VC08057587650069
MIO-4VM08057587650014
MIO-3VM08057587650007
MIO-5VM08057587650021
MIO-2YC08057587650120
MIO-4YC08057587650144
MIO-3YC08057587650137
MIO-5YC08057587650151
MIO-1YC08057587650113
MIO-4YM08057587650090
MIO-3YM08057587650083
MIO-5YM08057587650106
MIO-4CS08057587650274
MIO-3CS08057587650267
MIO-2CS08057587650250

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