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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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CATETERE FLESSIBILE — 1 UDI-DI variant, MDD (GEM SRL)

MD Atlas
GEM SRL

Data from EUDAMED, last updated May 30, 2026

CATETERE FLESSIBILE

B-G2-LPC3Z

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: GEM SRL

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: DD 60135036
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TUV Rheinland Italia SRL (1936)
Validity: Dec 13, 2023

Identity & classification

Basic UDI-DI: B-G2-LPC3Z
Device name: CATETERE FLESSIBILE
Device model: G2-LPC
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Oct 10, 2022

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

1 UDI-DI variant

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basicUdiUlid01GF0FNC6FM0BY69TGXRZTV46Y

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

G2-LPCD-G2-LPC3Z