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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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ARGUS LifePoint — 2 UDI-DI variants, MDR (SCHILLER AG)

MD Atlas
SCHILLER AG

Data from EUDAMED, last updated May 23, 2026

ARGUS LifePoint

761336500000001659

2 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: SCHILLER AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 761336500000001659
Device name: ARGUS LifePoint
Device model: ARGUS LifePoint
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: SCHILLER AG
SRN: CH-MF-000012722
Country: Switzerland
Email: info@schiller.ch
Phone: +41 41 766 42 42

Authorised representative

Name: SCHILLER Medizintechnik GmbH
SRN: DE-AR-000006934
Country: Germany
Phone: +49 89 629981 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQSCVTEF965X2KHA844QPNDE

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

ARGUS LifePoint07613365002676
ARGUS LifePoint 207613365002744