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.

ZOCCOLI RIUTILIZZABILI — 127 UDI-DI variants, MDR (GIMA SPA)

MD Atlas
GIMA SPA

Data from EUDAMED, last updated May 31, 2026

ZOCCOLI RIUTILIZZABILI

80232790000V90996500000D5

127 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: GIMA SPA

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: 80232790000V90996500000D5
Device name: ZOCCOLI RIUTILIZZABILI
Device model: ZOCCOLI RIUTILIZZABILI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: GIMA SPA
SRN: IT-MF-000011004
Country: Italy
Email: REGOLATORIO@GIMAITALY.COM
Phone: 029538541

Variants by status

UDI-DI variants

127 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

basicUdiUlid01KSQD4BMBZA20PQABWN72BVTV

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

2637108023279263718
2637208023279263725
2637308023279263732
2637408023279263749
2637508023279263756
2637608023279263763
2637708023279263770
2637808023279263787
2637908023279263794
2638008023279263800
2638108023279263817
2638208023279263824
2641108023279264111
2641208023279264128
2641308023279264135
2641408023279264142
2641508023279264159
2641608023279264166
2641708023279264173
2641808023279264180
2641908023279264197
2642008023279264203
2642108023279264210
2642208023279264227
2631108023279263114

1 2 3 4 5