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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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Coprispalle in lana — 7 UDI-DI variants, MDR (G.L.O. SRL)

MD Atlas
G.L.O. SRL

Data from EUDAMED, last updated May 30, 2026

Coprispalle in lana

805156628430CS

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: 805156628430CS
Device name: Coprispalle in lana
Device model: 430
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

7 UDI-DI variants

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Applied filters

basicUdiUlid01K9VK866HCYRHAVB35NV4ACDX

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

430 mis. 7°08051070431869
430 mis. 5°08051566281633
430 mis. 1°08051566281596
430 mis. 6°08051566281640
430 mis. 3°08051566281619
430 mis. 4°08051566281626
430 mis. 2°08051566281602