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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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Narlisim soluzione per uso nasale e… — 2 UDI-DI variants, MDR

MD Atlas
Laboratori Baldacci S.p.A.

Data from EUDAMED, last updated May 30, 2026

Narlisim soluzione per uso nasale e per aerosolterapia

8024785NARLSOL5Q

2 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: Laboratori Baldacci S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8024785NARLSOL5Q
Device name: Narlisim soluzione per uso nasale e per aerosolterapia
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: Laboratori Baldacci S.p.A.
SRN: IT-MF-000020509
Country: Italy
Email: infoeu@baldaccilab.com
Phone: +39 050313271

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01KRJQC18D2218D71AJ8DTYM07

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

222B08024785000040
222A 08024785000033