Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

MD0105.04 Tubing Sets Daypack Single… — 3 UDI-DI variants, MDR

MD Atlas
Oertli Instrumente AG

Data from EUDAMED, last updated May 23, 2026

MD0105.04 Tubing Sets Daypack Single Pump System

76300039MD010504T4

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76300039MD010504T4
Device name: —
Device model: MD0105.04 Tubing Sets Daypack Single Pump System
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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01K6356Y2DPTRRH26RKGPKG598

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

Daypack cassette Faros/CataRhex 3/Swisstech07630003910070
Daypack tubing set Faros/CataRhex 3/Swisstech07630003904383
I/A tubes for daypack tubing set07630003918915