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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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Rüsch Bronchoflex - Endotracheal Tube… — 2 UDI-DI variants, MDR

MD Atlas
Teleflex Medical

Data from EUDAMED, last updated May 24, 2026

Rüsch Bronchoflex - Endotracheal Tube Oral (Cuffed and Uncuffed)

08019020000000000000143KF

2 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: Teleflex Medical

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08019020000000000000143KF
Device name: Rüsch Bronchoflex - Endotracheal Tube Oral (Cuffed and Uncuffed)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Teleflex Medical
SRN: IE-MF-000015868
Country: Ireland
Email: orders.intl@teleflex.com
Phone: 353 (0) 9 06 46 08 00

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KPTVEBAG0G390C3S881J4D2A

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

Reinforced Endotracheal Tube, oral, cuffed14026704734242
Reinforced Endotracheal Tube, oral, uncuffed14026704734235