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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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105/SP — 22 UDI-DI variants, MDR (G.L.O. SRL)

MD Atlas
G.L.O. SRL

Data from EUDAMED, last updated May 30, 2026

105/SP

805156628105SPV2

22 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: 805156628105SPV2
Device name: —
Device model: 105/SP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 10, 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

22 UDI-DI variants

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Applied filters

basicUdiUlid01K9PC13MS0WNTAA9C421EXY21

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

105/SP08051566288069
105/SP08051566288083
105/SP08051566288076
105/SP08051566288038
105/SP08051566288007
105/SP08051566287994
105/SP08051566288021
105/SP08051566288045
105/SP08051566288014
105/SP08051566287987
105/SP08051566288052
105/FO/SPF08051566288250
105/FO/SPF08051566288304
105/FO/SPF08051566288267
105/FO/SPF08051566288243
105/FO/SPF08051566288281
105/FO/SPF08051566288205
105/FO/SPF08051566288229
105/FO/SPF08051566288274
105/FO/SPF08051566288236
105/FO/SPF08051566288298
105/FO/SPF08051566288212