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Gaymar

Regular price $229.99 USD
Regular price Sale price $229.99 USD
Sale Sold out

Condition: Used

Warranty: 30 - Warranty

OEM: Gaymar Industries Inc.

SKU#: PIC R BOX 2-2C

Quantity
Duties included. Shipping calculated at checkout.

For sale to qualified healthcare professionals, healthcare facilities, biomedical service organizations, and authorized purchasers only. This listing does not include medication, pharmaceuticals, syringes, needles, or prescription drugs.

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Powers On

Yes

Cosmetic

Good

Cosmetic Condition

New in box

Excellent

Good

Poor

Condition ratings are based on a visual inspection and functional testing when possible.

Overview

Description:

The Gaymar T/Pump TP-500 Heat Therapy Pump is a temperature control unit designed for use with compatible Gaymar heat therapy equipment. It features a compact pump configuration for circulating temperature-controlled fluid through compatible therapy systems.

Specifications:

Brand: Gaymar

Model: T/Pump TP-500

Product Type: Heat Therapy Pump

Function: Temperature Control

System: T/Pump

Application: Heat Therapy Equipment

Features:

Gaymar T/Pump TP-500 model

Heat therapy pump configuration

Temperature control functionality

Compact equipment design

Designed for compatible Gaymar therapy systems

Technical Details

BrandGaymar
CategoryHeat Therapy Pump
Medical DisciplinePhysical Therapy
ConditionUsed
Cosmetic ConditionGood
Powers OnYes
OEMGaymar Industries Inc.
SKUPIC R BOX 2-2C
Warranty30 - Warranty

Need This Product Certified Patient-Ready?

If you require this product to be patient-ready certified, you can request a quote. Inspection, testing, repair, electrical safety testing, and calibration services are available through A Biomedical Service, Inc.

ISO 9001:2015
ISO 14001:2015
ISO 45001:2018
👉 Learn more about the equipment certification process
⚠️ Safety & Biomedical Inspection Notice

Shipping & Receiving Notice

Medical equipment may require inspection, functional verification, calibration, preventive maintenance, safety testing, or other evaluations following transportation and before being placed into service.

Upon receipt, the purchaser is responsible for inspecting the equipment for any shipping damage and determining whether any inspection, testing, calibration, preventive maintenance, or certification is necessary based on the manufacturer's recommendations, the receiving facility's policies, and all applicable laws and regulations.

The equipment should not be placed into clinical service or used for patient care until the purchaser has verified that it is safe, appropriate, and compliant for its intended use.

Biomedical Inspection Notice

Medical equipment should be evaluated by qualified personnel before being placed into clinical service. Depending on the type of equipment, the evaluation may include, as applicable:

  • Electrical safety testing
  • Functional performance verification
  • Alarm verification (if applicable)
  • Battery inspection or replacement (if applicable)
  • Calibration verification (if applicable)
  • Preventive maintenance
  • Software configuration and system settings
  • Verification of compatible accessories, consumables, and disposables
  • Inspection for shipping or handling damage
  • Compliance with the manufacturer's recommendations
  • Compliance with the receiving facility's policies, procedures, and applicable regulatory requirements

Transportation, storage, handling, and installation may affect the performance of medical equipment. Reuse Medical recommends that the receiving facility inspect, test, and evaluate the equipment in accordance with the manufacturer's recommendations and the facility's biomedical engineering procedures before placing the equipment into clinical service or patient use.