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Overview
Datex-Ohmeda Tec 7 Sevoflurane Anesthesia Vaporizer | Pre-Owned
Description
The Datex-Ohmeda Tec 7 Sevoflurane Anesthesia Vaporizer is designed for controlled delivery of Sevoflurane anesthetic agent when used with a compatible anesthesia system.
This is pre-owned equipment. Unless otherwise noted, the equipment is intended for professional use and should be inspected, tested, and evaluated by qualified personnel before being placed into service.
NOTE: This unit has not been tested and is missing pieces/components (cord). Only the items shown in the photographs or specifically listed are included. Additional accessories, cables, controllers, processors, power supplies, manuals, software, licenses, consumables, or other components are not included unless expressly stated.
What's Included
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Datex-Ohmeda Tec 7 Sevoflurane Anesthesia Vaporizer
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Items/components shown in the photographs
Specifications
| Specification | Details |
|---|---|
| Manufacturer | Datex-Ohmeda |
| Model | Tec 7 |
| Reference / REF | 1175-9301-000 |
| Serial Number / SN | BEJS04276 |
| Product Type | Anesthesia Vaporizer |
| Anesthetic Agent | Sevoflurane |
| Condition | Pre-Owned |
| Testing Status | Not Tested |
| SKU | Mid Main Rack MMR-12 |
Features
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Tec 7 anesthesia vaporizer
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Configured for Sevoflurane
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Concentration adjustment dial
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Designed for use with compatible anesthesia equipment
Condition
Pre-owned and not tested. The unit may show normal cosmetic signs of prior use, including scratches, scuffs, label wear, or discoloration.
Please review all photographs carefully for the actual condition and included components.
Shipping & Receiving
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Professionally packaged for safe transport
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Buyer should inspect the shipment upon arrival
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Report any shipping damage promptly
Return Eligibility
See the product page and full Return & Refund Policy at reusemedicalequipment.com for applicable return terms.
Technical Details
| Brand | Datex-Ohmeda |
|---|---|
| Category | Anesthesia Vaporizer |
| Medical Discipline | Internal Medicine |
| Cosmetic Condition | Good |
| OEM | Datex-Ohmeda |
| SKU | Mid Main Rack MMR-11 |
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.
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.
