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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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Benda di garza orlata — 8 UDI-DI variants, MDR

MD Atlas
Gammadis Farmaceutici Srl

Data from EUDAMED, last updated May 31, 2026

Benda di garza orlata

805347080MEDBENDEQV

8 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: Gammadis Farmaceutici Srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805347080MEDBENDEQV
Device name: —
Device model: Benda di garza orlata
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Gammadis Farmaceutici Srl
SRN: IT-MF-000032982
Country: Italy
Email: import@gammadis.it
Phone: +39 0733 898117

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JXMBW23X4W1F2MJQ5TPE338Z

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

10714408053470801440
10714508053470801457
10714308053470801433
10714008053470801402
10713908053470801396
10714208053470801426
10714108053470801419
107144-107145-10714608053470801464