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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 spinale — 9 UDI-DI variants, MDR (G.L.O. SRL)

MD Atlas
G.L.O. SRL

Data from EUDAMED, last updated May 31, 2026

Ortesi spinale

805107043ORTOSPIN76

9 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: G.L.O. SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805107043ORTOSPIN76
Device name: Ortesi spinale
Device model: ORTOSPIN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 12, 2025

Manufacturer & authorised representative

Manufacturer

Name: G.L.O. SRL
SRN: IT-MF-000018554
Country: Italy
Email: info@glo-lab.it

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01K9W5S3VJCX4QCNZGSDW733WD

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

ORTOSPIN mis.XS08051070438530
ORTOSPIN mis.L08051070438561
ORTOSPIN mis.S08051070438547
ORTOSPIN mis.M08051070438554
ORTOSPIN/1 mis.S08051070439162
ORTOSPIN/1 mis.M08051070439179
ORTOSPIN/1 mis.L08051070439186
ORTOSPIN/1 mis.XS08051070439155
ORTOSPIN mis.XL08051070439117