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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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Breathing tubes — 5 UDI-DI variants, MDR (NDD Medizintechnik AG)

MD Atlas
NDD Medizintechnik AG

Data from EUDAMED, last updated May 23, 2026

Breathing tubes

764014219BreathingTubes6L

5 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: NDD Medizintechnik AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764014219BreathingTubes6L
Device name: Breathing tubes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KPVBWJGRAKW6KDFBQPFTAXD6

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

Spirette FA Pro/LAB (basic unit)07640142190646
Spirette FA Pro/LAB, 200 pcs box07640142190684
Spirette FA Pro/LAB, 50 pcs box07640142190660
Spirette M07640142190677
Spirette M (basic unit)07640142190271