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1 28

GE Healthcare

GE Dinamap V100 Vital Signs Patient Monitor With SpO₂ Sensor, NIBP Cuffs, Power Adapter & Patient Cables

$249.99 USD
$249.99 USD
Sale Sold out

Condition: Used

Warranty: 30 - Warranty

OEM: GE Healthcare

SKU#: BOX 20-2

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.

View full details

Powers On

Yes

Functional

Tested / Working

Cosmetic

Good

Functional Condition

New

Used

Non-functional

Biomed Certified

Cosmetic Condition

New in box

Excellent

Good

Poor

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

Overview

Description:

This GE DINAMAP V100 Vital Signs Patient Monitor is designed for routine patient monitoring in hospitals, clinics, and healthcare facilities. The system is supplied with a compatible SpO₂ sensor, NIBP cuffs, power adapter, and patient cables, providing a complete setup for monitoring essential patient parameters during clinical assessment.

Specifications:

  • Brand: GE Healthcare

  • Model: DINAMAP V100

  • Product Type: Vital Signs Patient Monitor

  • Function: Patient Vital Signs Monitoring

  • Application: Hospital, Clinical, and Healthcare Facilities

  • Included Accessories: SpO₂ Sensor, NIBP Cuffs, Power Adapter, Patient Cables

  • Form Factor: Portable/Benchtop Monitor

Features:

  • Designed for routine patient monitoring

  • Includes compatible SpO₂ sensor

  • Supplied with NIBP cuffs, patient cables, and power adapter

  • Suitable for clinical and healthcare environments

  • OEM patient monitoring equipment

Technical Details

BrandGE Healthcare
CategoryVital Signs Patient Monitor
Medical DisciplineInternal Medicine
ConditionUsed
Functional ConditionTested / Working
Cosmetic ConditionGood
Powers OnYes
OEMGE Healthcare
SKUBOX 20-2
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

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⚠️ 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.