Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The VWR 1110 Heated Immersion Circulator is a laboratory temperature control device designed for heating and circulating liquid baths in compatible laboratory environments. Its immersion circulator configuration combines heating and fluid circulation functions to support consistent temperature management during laboratory procedures. Operating on a 115V power supply at 60Hz, this unit is suitable for laboratory applications requiring controlled heating and circulation.
Specifications:
Brand: VWR
Model: 1110
Product Type: Heated Immersion Circulator
Equipment Type: Laboratory Temperature Control Equipment
Voltage: 115V
Frequency: 60Hz
Serial Number: 906247
Function: Liquid Heating and Circulation
Application: Laboratory Temperature Control
Features:
Heated immersion circulator design
Integrated heating and circulation functionality
Designed for laboratory liquid bath applications
Temperature control equipment configuration
Suitable for compatible laboratory workflows
Technical Details
| Brand | VWR |
|---|---|
| Category | Heated Immersion Circulator |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | VWR |
| SKU | ROW-3-108 |
| Warranty | 30 - 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.
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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.
