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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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ZENZERO — 1 UDI-DI variant, MDR (ITALPOL OTTICI SRL)

MD Atlas
ITALPOL OTTICI SRL

Data from EUDAMED, last updated May 31, 2026

ZENZERO

803321957SKIZZZENZEROAD

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: ITALPOL OTTICI SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803321957SKIZZZENZEROAD
Device name: ZENZERO
Device model: ZENZERO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: ITALPOL OTTICI SRL
SRN: IT-MF-000027587
Country: Italy
Email: info@italpolottici.it
Phone: +393391614150

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01JRJ3EY9TMSRJTH3ZKYY976ST

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

ZENZERO08033219572657