G-tubes
Hand Pump Assembly
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 Hand Pump Assembly
We do not have contact details for Mercury Enterprises, Inc. yet. Send a request and we will route it to the right person for your country.
Hand Pump Assembly 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 |
|---|---|---|---|
| 88-GCT501 | — | Not stated | Available |
FDA clearances
- 510(k) K222880 March 2023
Procedures that use g-tubes
Frequently asked questions
What is Hand Pump Assembly 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 Hand Pump Assembly?
Hand Pump Assembly is made by Mercury Enterprises, Inc.. It is listed under gastrostomy and gj tubes in our device library.
What sizes does Hand Pump Assembly come in?
The FDA device database does not list sizes for Hand Pump Assembly. Check the instructions for use or ask a Mercury Enterprises, Inc. representative.
Is Hand Pump Assembly MRI safe?
The FDA device database entry for Hand Pump Assembly does not state its MRI safety status. Check the labeling before MRI.
Is Hand Pump Assembly FDA cleared?
Hand Pump Assembly is covered by FDA submission K222880.
How do I contact a Mercury Enterprises, Inc. sales representative?
Mercury Enterprises, Inc. has not listed representatives on LA Vascular yet. Visit the Mercury Enterprises, Inc. 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.