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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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Cura della gola spray — 3 UDI-DI variants, MDR

MD Atlas
ABOCA S.P.A. SOCIETÀ AGRICOLA

Data from EUDAMED, last updated May 30, 2026

Cura della gola spray

8032472CUGOax122

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: ABOCA S.P.A. SOCIETÀ AGRICOLA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8032472CUGOax122
Device name: Cura della gola spray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: ABOCA S.P.A. SOCIETÀ AGRICOLA
SRN: IT-MF-000029499
Country: Italy
Email: regulatoryaffairs@aboca.it
Phone: +39 0575 7461

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01J03VBM9MH9WRDZV6CCX07P9H

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

0803247201561108032472015611
0803247202887108032472028871
Soin de la gorge spray08032472031062