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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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Glubran Tiss 2 — 3 UDI-DI variants, MDR (GEM SRL)

MD Atlas
GEM SRL

Data from EUDAMED, last updated May 30, 2026

Glubran Tiss 2

803190229Z

3 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

Legacy certificates

Certificate number: 0425-MDR-030094-00
Type: refdata.certificate-mdr-type.quality-assurance
Notified body: ICIM S.P.A. (0425)
Validity: Sep 12, 2024 → Sep 11, 2029

Identity & classification

Basic UDI-DI: 803190229Z
Device name: Glubran Tiss 2
Device model: G-NBOC2, G-NBOC2-25,G-NBOC2-35
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 31, 2024

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

3 UDI-DI variants

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Applied filters

basicUdiUlid01JBH353YFKGJBVH99BN3R19D3

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

G-NBOC208031902000197
G-NBOC2-3508031902000210
G-NBOC2-2508031902000227