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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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MD0105.02 Tubing Sets Single Pump… — 3 UDI-DI variants, MDR

MD Atlas
Oertli Instrumente AG

Data from EUDAMED, last updated May 23, 2026

MD0105.02 Tubing Sets Single Pump System Single Use

76300039MD010502SY

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: Oertli Instrumente AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76300039MD010502SY
Device name: —
Device model: MD0105.02 Tubing Sets Single Pump System Single Use
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Oertli Instrumente AG
SRN: CH-MF-000016175
Country: Switzerland
Email: info@oertli-instruments.com
Phone: +41 71 74742 00

Authorised representative

Name: Oertli Ophthalmedic Österreich GmbH
SRN: AT-AR-000003554
Country: Austria
Phone: +43 5572 22584

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K631PGKN91WPT3FJ5KQAK9AY

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

Tubing set Faros/CataRhex 3/Swisstech07630003904390
Tubing set Faros/CataRhex 3/Swisstech07630003910711
Tubing set Faros/CataRhex 3/Swisstech07630003909685