
PM Checklist Pack by Modality
Four modality-specific PM checklists — infusion pumps, monitors, ventilators, defibrillators — with pass/fail and reading capture on every step.
Store
Ready-to-use calibration logs, PM checklists, and AEM program templates — no SaaS signup required.

Four modality-specific PM checklists — infusion pumps, monitors, ventilators, defibrillators — with pass/fail and reading capture on every step.

Technician readings in, sign-off-ready pass/fail records out — the Calibration & Electrical Safety Test Log Kit against limits you set.

Structure your AEM justification the way a surveyor reads it — inclusion criteria, category rationale, and a program summary, all in your own words and numbers.

Device in, inspection and sign-off out — plus a manual recall/hazard-alert log you keep yourself, with no automated or live-fed data.

The full BiomedicalTechnology.com catalogue in one bundle — PM and calibration checklists, safety logs, competency records, and the audit-binder template.

Assets in, survey-ready registry out — the Equipment Inventory & Asset Registry Builder locks the column schema every other HTM tool reads from.

Score each asset by risk to justify PM inclusion and assign defensible maintenance intervals in your own words — every weight and threshold is yours to set.

Last-completed date in, next-due date out — the PM/Calibration Schedule Planner builds a filterable year of PM/calibration due dates by modality and interval.
Assignment, status, scheduled vs. due date, completion — the Work-Order Dispatch Tracker follows every job across your multi-client roster.
Log every PM, calibration, and repair per asset — the Service History Workbook tracks downtime, cost, and end-of-life replacement from your own records.
Client metrics in, roster readiness out — the Multi-Client Compliance Dashboard rolls up PM completion, overdue counts, and status across every client hospital.

Compile one client's PM, calibration, safety, AEM, and competency records into a date-range-scoped binder with a surveyor-ready TOC and readiness self-check.

Roster and assessments in, a survey-ready competency picture out — track BMET skills, CBET/CRES/CLES status, and expiring renewals in one workbook.
Log survey findings, assign owners and due dates, and track corrective actions through re-inspection and closure — one deficiency-to-closure workbook.

PM and QA checklists for CT, MRI, ultrasound, and X-ray — pass/fail and readings per step, rolled up into an imaging QA dashboard by modality.

Log dialysis-machine PM, water/dialysate quality against your own limits, and electrical-safety testing — with out-of-range readings flagged for survey files.

Log sterilizer PM, per-load cycles, and biological/chemical indicator results — cycle in, validation record out, every parameter your own.

An ASC-tuned equipment-compliance pack — PM and safety logs, a readiness self-check, and a survey binder set for the outpatient-surgery CMS context.

A single-site in-house biomed program in a box — inventory, PM/calibration and safety logs, and an editable equipment-management plan for a small hospital.

A full-length, editable Medical Equipment Management Plan and policy set — the standard program sections, written in your own words.

A plain-language PDF reference to EQ56/EQ103, Joint Commission EM, CMS CoP, and AEM concepts — each named, explained, and mapped to the matching store workbook.
This template is a documentation aid, not legal, regulatory, or accreditation advice. AAMI EQ56/EQ103, Joint Commission Environment of Care standards, and CMS Conditions of Participation are real published standards; you remain responsible for your own compliance determination.
Instant digital download · all sales final.
One-time purchase, instant download, and a buyer account created automatically so you can re-download at any time. No subscription and no signup step before checkout.
HTM Compliance Manager tracks PM schedules and calibration due-dates across every client hospital you service, and generates the audit binder these templates produce by hand.
Before you buy
They are documentation aids: structured records you fill in, built around what a Joint Commission or CMS surveyor typically asks an independent service organization (ISO) to produce. They do not make a compliance determination for you, and they are not legal, regulatory, or accreditation advice.
Where a template covers recalls or hazard alerts, it is a manual, technician-entered log. There is no automated feed, no live sync, and no FDA integration behind any product in this catalogue.