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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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UroFlex™ N — 3 UDI-DI variants, MDR (MAUNA KEA TECHNOLOGIES)

MD Atlas
MAUNA KEA TECHNOLOGIES

Data from EUDAMED, last updated May 19, 2026

UroFlex™ N

376018791NCM6E7

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: MAUNA KEA TECHNOLOGIES

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376018791NCM6E7
Device name: UroFlex™ N
Device model: UroFlex™ N
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: MAUNA KEA TECHNOLOGIES
SRN: FR-MF-000000835
Country: France
Email: ra@maunakeatech.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KH6G1X25CS0C3T73W4GWCH5Y

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

FP-1003803760187912103
FP-1003203760187912042
FP-1003703760187912097