
Datrend · Model vPad-353
Automated and Manual Electrical Safety Testing per IEC 62353, AS 3551, AAMI/ANSI ES-1 and IEC 60601 standards. USB, RS-232 and wireless communication. DA-COM RS-232 multi-device external control. Extensive internal storage. Unlimited user comments in test records. Complete test procedures available instantly. Integrated ECG & Arrhythmia Simulator. Automated Testing Sequences for defibrillators, infusion devices, patient monitors, and more. All Autosequences and Checklists are 100% editable for total procedural customization. Internal test record storage. Automatic “flagging” of test results that are outside of pre-established test limits. Prints test result reports & inspection stickers. Reduces paperwork, eliminates handwritten records, standardizes medical device testing. Increases quality and accuracy. Increases throughput – saves more than 50% over manual testing & hand-written records. Core element of MEI Test System. CMMS compatible.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Readings disagree with a reference standard, verification check outside tolerance.
Root cause: Normal drift - the instrument needs its scheduled factory / accredited calibration (at least every 12 months).
Symptoms: Dead unit, short battery life, will not charge.
Root cause: Depleted or aged battery, or a power / charger fault.
Symptoms: Open or intermittent readings, connection errors, a specific function fails.
Root cause: Worn or broken test leads, mains adapters, patient-lead adapters, or a sensor cable.
Symptoms: One parameter (leakage, insulation, ECG / SpO2 / IBP simulation, defib / pacer energy, ventilator flow / pressure, light / dose) errors or is out of range while others work.
Root cause: An internal source / measurement circuit fault on that channel.
Symptoms: The automation / logging software will not connect.
Root cause: USB cable / port or driver.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
At least every 12 months per the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Test-lead / adapter set | Periodic replacement | $$ | Easy |
| Battery | Periodic replacement | $$ | Easy |
| Calibration (factory / accredited) At least every 12 months per the manufacturer. | Frequent wear item | $$ | Easy |
| Communication cable | Periodic replacement | $ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
No documents available for this device yet.
From BioLab, for work done with this kind of equipment.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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