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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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O3IMS.View — 6 UDI-DI variants, MDR (O3 Enterprise srl)

MD Atlas
O3 Enterprise srl

Data from EUDAMED, last updated May 30, 2026

O3IMS.View

805750062VIEWFC

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: O3 Enterprise srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805750062VIEWFC
Device name: O3IMS.View
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: O3 Enterprise srl
SRN: IT-MF-000028709
Country: Italy
Email: info@o3enterprise.com
Phone: 0409828200

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JJ9NSF0VZVSEYC8P4VFP0ZNV

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

RELEASES-3908057500620179
MeriConnect08057500620193
O3IMS.View08057500620148
TESI.View08057500620209
WebScribe View08057500620162
ZEEROmed View08057500620155