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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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GLUTACK — 4 UDI-DI variants, MDR (GEM SRL)

MD Atlas
GEM SRL

Data from EUDAMED, last updated May 30, 2026

GLUTACK

80319026A9

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: GEM SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80319026A9
Device name: GLUTACK
Device model: GB-DS 30; GB-DS 60; GB-DS SH 30; GB-DS SH 30; GB-DS SH 60
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 24, 2023

Manufacturer & authorised representative

Manufacturer

Name: GEM SRL
SRN: IT-MF-000012892
Country: Italy
Email: info@gemitaly.it
Phone: +39 0584 391388/389784

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HG0VQQYNP985VZQ03DCS3608

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

GB-DS 6008031902000654
GB-DS 3008031902000647
GB-DS SH 6008031902000807
GB-DS SH 3008031902000791