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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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Flow Sensor — 4 UDI-DI variants, MDR (NDD Medizintechnik AG)

MD Atlas
NDD Medizintechnik AG

Data from EUDAMED, last updated May 23, 2026

Flow Sensor

764014219FlowSensorRW

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: NDD Medizintechnik AG

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 764014219FlowSensorRW
Device name: Flow Sensor
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: NDD Medizintechnik AG
SRN: CH-MF-000015550
Country: Switzerland
Email: support@ndd.ch
Phone: +41445126500

Authorised representative

Name: NDD Medizintechnik GmbH
SRN: DE-AR-000032322
Country: Germany
Phone: +41445126500

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRG8NHBWKACM6MW9RBZ94AVT

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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