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

MD Atlas
G.L.O. SRL

Data from EUDAMED, last updated May 31, 2026

Fascia tubolare in lana

805596537513HW

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: 805596537513HW
Device name: Fascia tubolare in lana
Device model: 513
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 19, 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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Export results

Applied filters

basicUdiUlid01KAE46T1DNWCZREWZVDZF183D

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

513, mis.108055965372398
513, mis.308055965372411
513, mis.608055965372442
513, mis.708055965372459
513, mis.408055965372428
513, mis.508055965372435
513, mis.208055965372404