Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

FLIPPERS FOR BINOCULAR CONFIRMATION — 19 UDI-DI variants, MDR

MD Atlas
CENTRO STYLE S.p.A.

Data from EUDAMED, last updated May 30, 2026

FLIPPERS FOR BINOCULAR CONFIRMATION

8058692SV03037

19 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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8058692SV03037
Device name: FLIPPERS FOR BINOCULAR 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

19 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01FYRM78HFB5P683KNW8YTXJPH

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

08335RK08058692187914
08337RK08058692187938
08334RK08058692187907
08341RK08058692187945
08342RK08058692187952
08332RK08058692187884
08336RK08058692187921
08338RK08058692187969
08333RK08058692187891
0833508019659083359
0833708019659083373
0833208019659083328
0833608019659083366
0833308019659083335
0834108058692102122
0833408058692102115
0833808019659083380
0833908019659083397
0834208058692102139