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Symbio

Regular price $699.99 USD
Regular price Sale price $699.99 USD
Sale Sold out

Condition: Used

Warranty: 30 - Warranty

OEM: Symbio

SKU#: CIR.R3-1

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.

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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 Symbio CS1201 ECG Code Simulator is a specialized simulation device designed for ECG and arrhythmia training applications. It provides a dedicated training-oriented configuration for simulating ECG code scenarios and is identified by model number CS1201.

Specifications:

Brand: Symbio

Model: CS1201

Product Type: ECG Code Simulator

Application: ECG Training

Training Type: Arrhythmia Training

Configuration: Simulation Device

Features:

Symbio CS1201 configuration

ECG code simulation

Arrhythmia training design

Dedicated simulation equipment

Training-oriented configuration

Technical Details

BrandSymbio
CategoryECG Code Simulator
Medical DisciplineIntensive Care Unit
ConditionUsed
Cosmetic ConditionGood
Powers OnYes
OEMSymbio
SKUCIR.R3-1
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.