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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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PORTA AGHI — 40 UDI-DI variants, MDR (GIMA SPA)

MD Atlas
GIMA SPA

Data from EUDAMED, last updated May 31, 2026

PORTA AGHI

80232790000L02050000000CH

40 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: 80232790000L02050000000CH
Device name: PORTA AGHI
Device model: PORTA AGHI
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

40 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSQAPMP92FT6DTVQ9PR2QQT1

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

2673208023279267327
2681908023279268195
2673308023279267334
2653908023279265392
2653008023279265309
2653108023279265316
2653208023279265323
2653508023279265354
2653308023279265330
2653408023279265347
2654008023279265408
2654108023279265415
2654208023279265422
2654408023279265446
2674108023279267419

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