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Overview
Description:
The ScripTalk 220-SN Network RFID Thermal Barcode Label Printer is a specialized printing device designed for producing thermal barcode labels and RFID-enabled labels in compatible labeling environments. Its thermal printing technology provides a printing solution for label generation, while the network connectivity configuration supports integration with compatible computer systems and network setups. The unit is designed for applications requiring organized label printing and identification.
Specifications:
Brand: ScripTalk
Model: 220-SN
Product Type: Network RFID Thermal Barcode Label Printer
Printer Type: Thermal
Printing Technology: Thermal Printing
Connectivity: Network
RFID Capability: RFID Label Support
Function: Barcode and RFID Label Printing
Application: Labeling / Identification Systems
Features:
Thermal barcode label printing design
RFID label support
Network connectivity configuration
Designed for compatible labeling systems
Suitable for identification and labeling applications
SKU : DA42-ITEM-X
Technical Details
| Brand | ScripTalk |
|---|---|
| Category | Network RFID Thermal Barcode Label Printer |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | ScripTalk |
| SKU | DA42-ITEM-X - P |
| 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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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.
