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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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Polsino steccato ambidestro — 12 UDI-DI variants, MDR (G.L.O. SRL)

MD Atlas
G.L.O. SRL

Data from EUDAMED, last updated May 30, 2026

Polsino steccato ambidestro

805596537605B9V

12 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: 805596537605B9V
Device name: Polsino steccato ambidestro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 24, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KAV0DHPEW6ZTDBZHXSV4W862

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

6029, mis.S08055965377768
6029, mis.XL08055965377799
6022, mis.M08055965377737
6022, mis.XL08055965377751
605/B, mis.XL08055965376266
6029, mis.L08055965377782
6022, mis.S08055965377720
6022, mis.L08055965377744
605/B, mis.S08055965376235
605/B, mis.L08055965376259
6029, mis.M08055965377775
605/B, mis.M08055965376242