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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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iPeeWell Uroflowmeter — 2 UDI-DI variants, MDR (iPeeWell d.o.o.)

MD Atlas
iPeeWell d.o.o.

Data from EUDAMED, last updated May 31, 2026

iPeeWell Uroflowmeter

50700043220IUFM1D7

2 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: iPeeWell d.o.o.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 50700043220IUFM1D7
Device name: iPeeWell Uroflowmeter
Device model: IUFM1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: iPeeWell d.o.o.
SRN: SI-MF-000043692
Country: Slovenia
Email: info@ipeewell.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMK4VX44E97949MX5P85E1ZC

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

iPeeWell Uroflowmeter HOME05070004322007
iPeeWell Uroflowmeter PRO05070004322014