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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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TUBI AMNIOSCOPICI — 3 UDI-DI variants, MDR (GIMA SPA)

MD Atlas
GIMA SPA

Data from EUDAMED, last updated May 31, 2026

TUBI AMNIOSCOPICI

8023279Z1202908562000008H

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: GIMA SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8023279Z1202908562000008H
Device name: —
Device model: TUBI AMNIOSCOPICI
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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSQ24P3FQB1P5JMF82P3GRT9

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

2997108023279299717
2997208023279299724
2997308023279299731