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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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GIOVE 4 — 2 UDI-DI variants, MDR (FISIOTECH srl)

MD Atlas
FISIOTECH srl

Data from EUDAMED, last updated May 30, 2026

GIOVE 4

8050593941118DSX

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: FISIOTECH srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8050593941118DSX
Device name: GIOVE 4
Device model: SERIE TOP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2024

Manufacturer & authorised representative

Manufacturer

Name: FISIOTECH srl
SRN: IT-MF-000028185
Country: Italy
Email: info@fisiotech.com
Phone: +39 0 438 47 03 42

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HY3DQJH1CZ61NME0X984WXVT

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

GIOVE 4 COUCH80505939400632
GIOVE 4 COUCH80505939400700