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Welch Allyn

Regular price $549.99 USD
Regular price Sale price $549.99 USD
Sale Sold out

Condition: Used

Warranty: 30 - Warranty

OEM: Welch Allyn

SKU#: BOX 20-1

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.

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 Welch Allyn Vital Signs Monitor 6000 Series is a patient monitoring system designed to measure and display essential vital signs in clinical and healthcare environments. The unit includes patient cables and blood pressure cuffs, making it suitable for routine patient assessment and monitoring in hospitals, clinics, and medical facilities.

Specifications:

  • Brand: Welch Allyn

  • Series: 6000 Series

  • Reference Number: 64MTXX

  • Product Type: Vital Signs Monitor

  • Function: Patient Vital Signs Monitoring

  • Application: Hospital, Clinical, and Healthcare Facilities

  • Included Accessories: Patient Cables, Blood Pressure Cuffs

  • Form Factor: Benchtop/Mobile Clinical Monitor

Features:

  • Designed for routine vital signs monitoring

  • Includes patient cables and blood pressure cuffs

  • Suitable for clinical and healthcare environments

  • User-friendly monitoring interface

  • OEM patient monitoring equipment

Technical Details

BrandWelch Allyn
CategoryVital Signs Monitor
Medical DisciplineInternal Medicine
ConditionUsed
Functional ConditionTested / Working
Cosmetic ConditionGood
Powers OnYes
OEMWelch Allyn
SKUBOX 20-1
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.