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Fisher Scientific

السعر الاعتيادي $159.99 USD
السعر الاعتيادي سعر البيع $159.99 USD
مبيع نفد المخزون

Condition: Used

Warranty: 30 - Warranty

OEM: Fisher Scientific

SKU#: ROW-3-111

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 Fisher Scientific Isotemp 110 Laboratory Water Bath is a temperature-controlled laboratory heating device designed for maintaining liquid samples at selected temperatures in compatible laboratory environments. Its water bath configuration provides a controlled heating setup for routine sample preparation and laboratory procedures. Operating at 50/60Hz with a rated current of 2.8A, this unit is suitable for general laboratory applications requiring consistent liquid heating.

Specifications:

Brand: Fisher Scientific
Product Line: Isotemp
Model: 110
Product Type: Laboratory Water Bath
Catalog Number: 15-460-11
Current: 2.8A
Frequency: 50/60Hz
Function: Liquid Heating and Temperature Control
Application: Laboratory Sample Preparation

Features:

Isotemp 110 water bath design
Temperature-controlled heating configuration
Designed for laboratory sample preparation
Suitable for liquid heating applications
Compatible with routine laboratory workflows

Technical Details

BrandFisher Scientific
CategoryLaboratory Water Bath
Medical DisciplineLaboratory
ConditionUsed
Cosmetic ConditionGood
Powers OnYes
OEMFisher Scientific
SKUROW-3-111
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.