Medtronic 49351 Instructions for Use

Cardioblate™ Gemini™-s 49351

Surgical Ablation Device

Instructions for Use

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.

The following list includes trademarks or registered trademarks of Medtronic in the United States and possibly in other countries. All other trademarks are the property
of their respective owners.

Cardioblate, Covidien, Gemini, LigaSure, Medtronic, TissueFect, Valleylab

Explanation of symbols on package labeling

Refer to the device labeling to see which symbols apply to this product.

Nonpyrogenic

Sterilized using ethylene oxide

Do not reuse

Do not resterilize

Use-by date

Lot number

Quantity

Consult instructions for use at this website

For US audiences only

Upper limit of temperature

Humidity limitation

Date of manufacture

Catalog number

Manufacturer

Contains di(2-ethylhexyl)phthalate (DEHP)

Do not use if package is damaged

Type CF applied part

3

Figure 1.

1 Rigid, slim-line jaws with guide attachments

EN

2 6.3 cm (2.49 in) electrodes embedded in a porous polymer
3 RF trigger
4 Malleable neck
5 Handle
6 Handle lock release
7 Molded hand piece
8 Saline fluid delivery tubing 304.8 cm (120 in) in length with a female luer for connection to standard IV tubing systems
9 Electrical cable 304.8 cm (120 in) in length that terminates into a multi-pin connector

4