Used GYRUS ACMI G3

Used
In stock
USA
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Product Details

GYRUS ACMI
G3
Electrosurgical Unit
06.05.2024
55

Product Description

Gyrus ENT RF Workstation Somnoplasty 761008
G3 Generator
Plasmakinetic PK”
Plasmacision PC”
TCRF v2.12
Plasmablend v 1.09

System is MISSING back left rubber 'foot' on the bottom of console

Has ‘PK’ and ‘PC’ connectors that many units do not have.

Remanufactured by Gyrus at some point. ID tag gives manufacture date as 10/2004. Do not know if this is original date or remanufacture date.

Do NOT know if this Footswitch will work with this console but connector fits so we are including it.

Metal housing has two dents on back left quarter edge.
Unit has scuffs and scratches.
Keypad membrane and Display are in great condition.
Unit powered on but no further testing can be done due to lack of accessories and knowledge.

Tag data states:
Plasmakinetic ‘PK’ Output:
315-480kHz 200W / 150 ohms (?). Int 10s/30s
Plasmacision ‘PC’ Output:
315-480KHz 200W / 150 ohms (?). Int 20s/30s
‘TCRF’ Output:
445kHz 2 X 15W / 100 ohms (?)
Model No.: 761008 G3 Generator
Gyrus ENT PART No.: 7035-3001

Disclaimer: This item is sold as is, no warranties implied. The item described and/or pictured offered here is in no way certified for, recommended for, or offered for any specific use. The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or coincidental, associated in any way with this equipment. It is the sole responsibility of the purchaser to obtain qualified help to ensure the proper functioning, calibration, and safety (mechanical, electrical, etc.) of this equipment. The purchaser by biding on this item, indicates their knowledge of an agreement to the terms of this disclaimer. This item is sold completely as is/ as shown with no warranty either expressed or implied. The sale of this item maybe subject to regulations by the U.S. Food and Drug Administration, state and local regulatory agencies. If you should have questions about legal obligations, you should consult with the U.S. Food and Drug Administration.