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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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OTOSCOPI — 22 UDI-DI variants, MDR (GIMA SPA)

MD Atlas
GIMA SPA

Data from EUDAMED, last updated May 31, 2026

OTOSCOPI

8023279Z1214900600000002X

22 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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8023279Z1214900600000002X
Device name: OTOSCOPI
Device model: OTOSCOPI
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

22 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSQHGVYX1NR6NNZDDN8APQK0

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

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3152108023279315219
3152008023279315202
3152208023279315226
3152508023279315257
3152308023279315233
3152408023279315240
3151808023279315189
3151308023279315134
3152608023279315264
3151108023279315110
3153508023279315356
3144108023279314410
3144008023279314403
3147508023279314755
3147408023279314748
3143608023279314366
3143708023279314373
3143508023279314359
3159208023279315929
3159108023279315912
3159308023279315936