CARDIOVIT CS-300

Organization name

SCHILLER AG

SRN

CH-MF-000012722

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW017

  The applied part of CARDIOVIT CS-300 or the MS-12 BT is CF classified. It is defibrillation protected only when the SCHILLER original patient cable is used. As a precaution however, when possible remove the electrodes before defibrillation.  Ensure that the patient is informed about the procedure for stress testing and is aware of the risks (for example, of falling on a running treadmill). Ensure the patient is aware of the location and use of the emergency stop knob when using a treadmill.  Do not touch the unit casing during defibrillation.  To ensure patient safety, none of the electrodes, including the neutral electrode, nor the patient or any person with simultaneous patient contact, must come in contact with conductive parts, even when these are earthed

Primary placement in Austria; available across 2 countries total.

Trade name

CARDIOVIT CS-300

UDI-DI code

07613365004052

Basic UDI-DI

761336500000002356

Reference / catalog number

07613365004052

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Z12050301GENERAL PURPOSE ELECTROCARDIOGRAPHS

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

Certificate health across this manufacturer's portfolio.