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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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ORTESI TORACO-LOMBO-SACRALI -… — 74 UDI-DI variants, MDR

MD Atlas
F.G.P. s.r.l.

Data from EUDAMED, last updated May 31, 2026

ORTESI TORACO-LOMBO-SACRALI - IPERESTENSORI

803348865Y06030902CR

74 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: F.G.P. s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803348865Y06030902CR
Device name: ORTESI TORACO-LOMBO-SACRALI - IPERESTENSORI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: F.G.P. s.r.l.
SRN: IT-MF-000043862
Country: Italy
Email: jennifer.adami@fgpsrl.it
Phone: 0458600867

Variants by status

UDI-DI variants

74 UDI-DI variants

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Applied filters

basicUdiUlid01JVKKJP32GHR6Y30VFS5YE4PM

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

No registered UDI-DI variants for this device family.