تجاوز إلى معلومات المنتج
1 من 8

Stryker

السعر الاعتيادي $649.99 USD
السعر الاعتيادي سعر البيع $649.99 USD
مبيع نفد المخزون

Condition: Used

Warranty: 30 - Warranty

OEM: Stryker

SKU#: DA43-ITEM-O

الكمية

Standard processing time for most equipment is 1 to 3 business days. For more details, please visit our Shipping Policy.

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.

عرض التفاصيل كاملة

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 Stryker 5100-1 TPS Total Performance System Arthroscopy Console is an equipment control unit designed for use with compatible Stryker surgical and arthroscopy system components. Its electronic console configuration provides a centralized interface for managing supported equipment functions and integrating compatible accessories. The TPS system is designed for use in suitable surgical equipment setups and clinical environments.

Specifications:

Brand: Stryker
Model: 5100-1
Product Line: TPS Total Performance System
Product Type: Arthroscopy Console
Equipment Type: Surgical Equipment Control Console
System Type: Total Performance System
Function: Equipment Control and System Integration
Application: Compatible Stryker Surgical Systems

Features:

TPS Total Performance System configuration
Electronic equipment control console
Designed for compatible Stryker accessories
Centralized system interface
Suitable for compatible surgical equipment setups

Technical Details

BrandStryker
CategoryTPS Total Performance System
Medical DisciplineGeneral Surgery
ConditionUsed
Cosmetic ConditionGood
Powers OnYes
OEMStryker
SKUDA43-ITEM-O
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

Related Products

No similar items available.

⚠️ 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.