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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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Ultrason gel — 13 UDI-DI variants, MDR (Naqi NV)

MD Atlas
Naqi NV

Data from EUDAMED, last updated May 23, 2026

Ultrason gel

542502989USUN

13 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Naqi NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 542502989USUN
Device name: Ultrason gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: Naqi NV
SRN: BE-MF-000001241
Country: Belgium
Email: info@naqi.com
Phone: +32(0)13460190

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01GPR700E1A1PNRMW3Z99VZ9H8

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

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Enraf Nonius Ultrasound Contactgel 250ml05425029892828
Enraf Nonius Ultrasound Contactgel bulk15425029892825
GU-US505425029892507
Gymna Contact gel 200 ml15425029892818
Gymna Contact gel 200 ml05425029892811
GU-US50005425029892538
GU-US50015425029892535
US505425029890206
NAQI UltraSon Gel 500 ml shipper15425029890197
US50005425029890190