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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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Organization name
UDI-DI code
Reference / catalog number

ARGUS LifePoint 2 — Class I MDR by SCHILLER AG

MD Atlas
SCHILLER AG

EUDAMED last updated this device on May 4, 2026

ARGUS LifePoint 2

761336500000001659

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHILLER AG
UDI-DI code: 07613365002744
Reference / catalog number: 2.100870

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Manufacturer information

Organization name: SCHILLER AG
SRN: CH-MF-000012722
Manufacturer status: Active

Related devices

PB-3000 Var. 476133650000000014UOn the market PB-3000 Var. 7, sub-variant: C (main device 3.921008)76133650000000014UOn the market ARGUS LifePoint761336500000001659On the market ARGUS PB-1000B-07613365000092On the market ARGUS PB-1000B-07613365000085On the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: ARGUS LifePoint 2
UDI-DI code: 07613365002744
Basic UDI-DI: 761336500000001659
Reference / catalog number: 2.100870
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The LifePoint is used as a guide in practice of cardiopulmonary resuscitation (CPR) at patients with suspected cardiac arrest, and where CPR can be performed with the heel of the hand. When attached to the chest of the patient, the Sensor provides real-time feedback on the performed CPR compressions with measurements of depth, rate and recoil for each single compression.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C03010301CARDIOPULMONARY SUPPORT KITS (C.P.S. AND ECMO)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

G10 041505 0132Issued
Quality management systemNotified body: 0123Expiry: Nov 11, 2026