Model note · ECG

SCHILLER CARDIOVIT AT-102 G2

Name: SCHILLER CARDIOVIT AT-102 G2
Brand: SCHILLER CARDIOVIT

The CARDIOVIT AT-102 G2 is SCHILLER's second generation 12 channel resting electrocardiograph, following the earlier AT-102 range. It records, analyses, displays, stores and transmits ECGs for all patient groups, with optional ETM interpretation, rhythm recording, basic exercise testing and spirometry through the SpiroScout SP plus sensor. It is a compact desktop or trolley unit with an 8 inch colour screen, a sealed keyboard, an A4 thermal printer, a lithium-ion battery and built in LAN and Wi-Fi for PDF, HL7 and DICOM export.

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The model

Maker, model and type.

Maker: SCHILLER AG
Model: CARDIOVIT AT-102 G2
Device type: ECG
Main document: Open the public document

Key specifications

What the public record says.

Item	Value	Source
Sampling rate and bandwidth	32,000 Hz sampling; 250 Hz bandwidth	Source
Patient input	Fully floating and isolated, Type CF, defibrillation protected only with the original SCHILLER patient cable	Source
Filters	Myogram filter off, 25, 40, 150 or 250 Hz (250 Hz means filter off); adaptive digital 50 or 60 Hz mains filter	Source
Printer	Thermal head, 8 dots/mm amplitude and 40 dots/mm time axis at 25 mm/s; 210 mm Z-fold paper; 5, 12.5, 25 or 50 mm/s; 5, 10 or 20 mm/mV	Source
Memory	At least 350 ECGs, 100 resting rhythm recordings and 10 exercise ECGs	Source
Display	8 in backlit LCD, 1024 x 768	Source
Power and battery	100 to 240 VAC, 50/60 Hz, 64 VA maximum; lithium-ion 10.8 V 6.9 Ah (units from 05/2018 to 04/2020 used 11.25 V 6.4 Ah); about 8.5 hours normal use; about 4 hours to full charge with the unit off	Source
Interfaces	ECG cable port, potential equalisation, 1 Gbit LAN, 2 USB, 2 RS-232; dual band 802.11 a/b/g/n Wi-Fi with WPA2	Source
Size, weight and protection	384 x 319 x 90 mm, about 4.5 kg with paper; Class I; IP20, not for outdoor use	Source
Operating environment	10 to 40 C, 15 to 95% RH non-condensing, 700 to 1060 hPa	Source
FDA clearance	K183425, CARDIOVIT AT-102 G2, product code DPS, Class II, decided 2 March 2020	Source

Recalls

Recalls.

This note lists no recalls. Check the FDA recall database for the latest record.

Safety

Safety warnings from the record.

Defibrillation protection applies only with the original SCHILLER patient cable; remove electrodes before defibrillating where possible and do not touch the unit during the shock. Source
With the Wi-Fi module switched on, keep the device at least 20 cm from an implanted pacemaker. Source
Do not use the unit if its earth connection is suspect or the mains lead, power supply or device may be damaged, and replace fuses only with the original type and rating. Source
If liquid is spilt on the unit, disconnect mains, wipe it and have it checked before further use. Source
After heavy artefact or lead-off the displayed heart rate may be unreliable. Source

Sources

Where this note comes from.

Not covered: Swapped to the AT-102 G2 because no public AT-102 plus manual or data sheet was found; the AT-102 plus is the earlier model and its details are not covered. The K183425 PDF holds only the decision letter and indications, with no technical summary. The user guide is a distributor hosted copy; no SCHILLER service handbook was publicly available, so there are no internal part, calibration or numeric error code details, and the error entries are on screen messages. No recall names the AT-102 G2; recall Z-2734-2024 (high frequency artefact) concerns the CARDIOVIT AT-180, which shares the K183425 clearance, and was left out as a different model. MAUDE has only one report for this brand name, too few to show a trend. The US page quotes 10 minute rhythm recording while the 2025 brochure says 20 minutes, so rhythm length was left out of specs.

BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.

ECG