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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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Estensore dorsale — 7 UDI-DI variants, MDR (G.L.O. SRL)

MD Atlas
G.L.O. SRL

Data from EUDAMED, last updated May 31, 2026

Estensore dorsale

805156628310CF

7 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: 805156628310CF
Device name: Estensore dorsale
Device model: 310
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 14, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KA189YC73VKTEYKFA2SKFJD4

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

310, mis.XXL08051566280889
310, mis.XXXL08051070435782
310, mis.L08051566280865
310, mis.XL08051566280872
310, mis.XS08055965379922
310, mis.M08051566280858
310, mis.S08051566280841