G-tubes
BOEHRINGER ViSiGi Lux 32 Fr
by Boehringer Laboratories, LLC
A thin, flexible, hollow cylinder with an inflatable balloon at the distal end designed to be inserted into a patient's stomach through the mouth and oesophagus to create and size a gastric pouch typically for a bariatric gastric surgical procedure (e.g., sleeve gastrectomy, gastric banding). The proximal end may include a check valve and connects to a syringe, typically included, intended to inflate the balloon to a predetermined volume; fluid suction/irrigation ports are provided at the distal end. This is a single-use device.
Where to buy BOEHRINGER ViSiGi Lux 32 Fr
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BOEHRINGER ViSiGi Lux 32 Fr models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 5332SB | Catheter Gauge 32 Fr | Not stated | Available |
| 5336SB | Catheter Gauge 36 Fr | Not stated | Available |
| 5340SB | Catheter Gauge 40 Fr | Not stated | Available |
Procedures that use g-tubes
Frequently asked questions
What is BOEHRINGER ViSiGi Lux 32 Fr used for?
A thin, flexible, hollow cylinder with an inflatable balloon at the distal end designed to be inserted into a patient's stomach through the mouth and oesophagus to create and size a gastric pouch typically for a bariatric gastric surgical procedure (e.g., sleeve gastrectomy, gastric banding). The proximal end may include a check valve and connects to a syringe, typically included, intended to inflate the balloon to a predetermined volume; fluid suction/irrigation ports are provided at the distal end. This is a single-use device.
Who makes BOEHRINGER ViSiGi Lux 32 Fr?
BOEHRINGER ViSiGi Lux 32 Fr is made by Boehringer Laboratories, LLC. It is listed under gastrostomy and gj tubes in our device library.
What sizes does BOEHRINGER ViSiGi Lux 32 Fr come in?
Sizes listed for BOEHRINGER ViSiGi Lux 32 Fr: Catheter Gauge: 32–40 Fr. Confirm availability with the manufacturer's instructions for use.
Is BOEHRINGER ViSiGi Lux 32 Fr MRI safe?
The FDA device database entry for BOEHRINGER ViSiGi Lux 32 Fr does not state its MRI safety status. Check the labeling before MRI.
Is BOEHRINGER ViSiGi Lux 32 Fr FDA cleared?
BOEHRINGER ViSiGi Lux 32 Fr is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Boehringer Laboratories, LLC sales representative?
Boehringer Laboratories, LLC has not listed representatives on LA Vascular yet. Visit the Boehringer Laboratories, LLC company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.