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Organization name
UDI-DI code
Reference / catalog number

CARDIOVIT AT-180 — Class IIa MDR by SCHILLER AG

MD Atlas
SCHILLER AG

EUDAMED last updated this device on Jun 11, 2025

CARDIOVIT AT-180

76133650000000085A

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHILLER AG
UDI-DI code: 07613365002775
Reference / catalog number: 3.920570

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Manufacturer information

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

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW017
This device is CF classified and defibrillation protected only when the original patient cable is used. However, as a safety precaution when possible, remove electrodes before defibrillation.
CW011
Consult the warning and safety information in the instructions for use

Market distribution

Primary placement in Slovenia; available across 2 countries total.

Country	On market since	Until
SloveniaPrimary placement		Still on market
Finland		Still on market

Device identification

Trade name: CARDIOVIT AT-180
UDI-DI code: 07613365002775
Basic UDI-DI: 76133650000000085A
Reference / catalog number: 3.920570
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: The CARDIOVIT AT-180 is an electrocardiograph intended to be used by trained operators under the direct supervision of a licensed physician in healthcare facilities to acquire ECG signals from body surface electrodes, record, analyse, display and print ECGs to support diagnosis of cardiovascular diseases in adult and paediatric patients at rest or undergoing exercise stress testing.
Additional information URL: https://www.schiller.ch/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12050301GENERAL PURPOSE ELECTROCARDIOGRAPHS

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

Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

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