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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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Nosiboo Pro — 4 UDI-DI variants, MDR (Attract Kft.)

MD Atlas
Attract Kft.

Data from EUDAMED, last updated May 24, 2026

Nosiboo Pro

5999885976PRO38

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: Attract Kft.

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Device characteristics

Active device

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 5999885976PRO38
Device name: Nosiboo Pro
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2023

Manufacturer & authorised representative

Manufacturer

Name: Attract Kft.
SRN: HU-MF-000004252
Country: Hungary
Email: quality@nosiboo.com
Phone: +3672551642

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01H0PZW8HGDMNR3B4T0A6CD0ND

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

NO-01-0105999885976003
NO-01-0305999885976041
NO-01-0405999861015306
NO-01-0205999885976010