Description
Cook Medical G34161 - SNARE, SONNET, POLYPEC, 7F, 3X4.5CM, SSH-28-S, 10/BX
Sonnet Short-Throw Polypectomy Snare
A monopolar electrosurgical device used with an electrical unit for endoscopic polypectomy.
The Sonnet Polypectomy Snare is a monopolar electrosurgical device used with an electrosurgical unit for endoscopic polypectomy. This device is supplied sterile and intended for single use only.
| Order Number | Reference Part Number | Sheath Size Fr | Snare Size (cm) | Snare Type | Minimum Accessory Channel (mm) |
Cord | Box Quantity |
| G34161 | SSH-28-S | 7 | 3 x 4.5 | hexagonal | 2.8 | Active cord available separately. | 10 |
NOTES
- Do not use this device for any purpose other than the stated intended use.
- Inventory rotation of sterile products is essential. Verify the expiration date on the package label prior to using the product. If the expiration date has lapsed, do not use.
- If the product package is open or damaged when received, do not use this device.
- Cook devices must be stored in a dry location, away from temperature extremes.
Contraindications
- Contraindications include those specific to the primary endoscopic procedure to be performed in gaining access to the polypectomy site.
- Contraindications to polypectomy include, but are not limited to: coagulopathy and insufficiently prepped bowel.
Potential Complications
Potential complications associated with gastrointestinal endoscopy include, but are not limited to: perforation, hemorrhage, aspiration, fever, infection, hypotension, allergic reaction to medication, respiratory depression or arrest, cardiac arrhythmia or arrest. Complications which can occur with endoscopic polypectomy include, but are not limited to: transmural burns, thermal injury to the patient, explosion.
Precaution
The coordination of endoscope accessory channel size with compatible devices is essential in order to obtain optimal results during a procedure. Please refer to the product package label for the minimum channel size required for this device.=
Cautions
U.S. Federal Law restricts this device to sale by or on the order of a physician.