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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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Elettrodi a coppetta — 2 UDI-DI variants, MDR

MD Atlas
GIUNTA ERASMO s.a.s. di Ing. Giovanni Giunta & C.

Data from EUDAMED, last updated May 30, 2026

Elettrodi a coppetta

805600049E108ZA

2 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: GIUNTA ERASMO s.a.s. di Ing. Giovanni Giunta & C.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805600049E108ZA
Device name: Elettrodi a coppetta
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: GIUNTA ERASMO s.a.s. di Ing. Giovanni Giunta & C.
SRN: IT-MF-000030841
Country: Italy
Email: giunta@giuntasas.eu
Phone: +39024694875

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JXCNH5W9GM679M6TNEWVPWHW

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

E108/V-15008056000490237
E108/V08056000490220