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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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BINOCULAR FLIPPER FOR VISUS CONFIRMATION — 3 UDI-DI variants, MDR

MD Atlas
CENTRO STYLE S.p.A.

Data from EUDAMED, last updated May 30, 2026

BINOCULAR FLIPPER FOR VISUS CONFIRMATION

8058692SV02034

3 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: CENTRO STYLE S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8058692SV02034
Device name: BINOCULAR FLIPPER FOR VISUS CONFIRMATION
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: CENTRO STYLE S.p.A.
SRN: IT-MF-000005996
Country: Italy
Email: lmarchi@centrostyle.it

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FYRGNA5BFX6AWX57HWCXWRYX

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

08326A08058692104294
0832508019659083250
08326B08058692104300