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GCA Corporation

Regular price $179.99 USD
Regular price Sale price $179.99 USD
Sale Sold out

Condition: Used

Warranty: 30 - Warranty

OEM: GCA Corporation

SKU#: DA431-ITEM-G

Quantity

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.

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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 GCA Corporation 25 Precision Scientific Reciprocal Shaking Water Bath Cat # 66800-26 is a laboratory temperature control and mixing device designed for use in compatible laboratory environments. Its reciprocal shaking mechanism provides controlled back-and-forth movement for sample mixing, while the water bath configuration supports temperature-controlled liquid applications. This unit combines heating and agitation functionality in a laboratory equipment setup suitable for sample preparation and general laboratory workflows.

Specifications:

Brand: GCA Corporation
Product Line: Precision Scientific
Model: 25
Product Type: Reciprocal Shaking Water Bath
Catalog Number: 66800-26
Equipment Type: Laboratory Water Bath
Operation: Reciprocal Shaking
Function: Temperature Control and Sample Agitation
Application: Laboratory Sample Preparation

Features:

Reciprocal shaking mechanism
Integrated water bath configuration
Temperature control functionality
Designed for laboratory sample mixing
Suitable for compatible laboratory workflows

Technical Details

BrandGCA Corporation
CategoryReciprocal Shaking Water Bath
Medical DisciplineBiological Laboratory
ConditionUsed
Cosmetic ConditionGood
Powers OnYes
OEM GCA Corporation
SKUDA431-ITEM-G
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.