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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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MŰORR AirBridge — 4 UDI-DI variants, MDR

MD Atlas
Pharmico Medical Korlátolt felelősségi társaság - MF

Data from EUDAMED, last updated May 24, 2026

MŰORR AirBridge

5996617MUORRFP

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: Pharmico Medical Korlátolt felelősségi társaság - MF

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5996617MUORRFP
Device name: MŰORR AirBridge
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: Pharmico Medical Korlátolt felelősségi társaság - MF
SRN: HU-MF-000018352
Country: Hungary
Email: fmocsar@pharmicomedical.hu

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JSGV41051VRK6FNATDMZY41D

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

www.discountmed.hu05996617000838
AB-571005996617000890
www.discountmed.hu05996617000845
www.discountmed.hu05996617000852