G-tubes
Moss
A thin, flexible, percutaneous, hollow tube which may include additional external components (e.g., external tubing, syringe) intended to be percutaneously inserted into the stomach to feed a patient with a physical disability that prevents oral feeding (e.g., a birth defect of the stomach), and/or provide drainage/decompression of the stomach when it is necessary to bypass an obstruction of the stomach outlet into the small intestine. Although noninvasive disposable enteral feeding components may be included, surgical instruments and pharmaceutical agents are not included. This is a single-use device.
Where to buy Moss
We do not have contact details for Moss Tubes, Inc. yet. Send a request and we will route it to the right person for your country.
Moss 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 |
|---|---|---|---|
| 5-17719 | Catheter Gauge 18 Fr | Not stated | Available |
FDA clearances
- 510(k) K990389 March 1999
Procedures that use g-tubes
Frequently asked questions
What is Moss used for?
A thin, flexible, percutaneous, hollow tube which may include additional external components (e.g., external tubing, syringe) intended to be percutaneously inserted into the stomach to feed a patient with a physical disability that prevents oral feeding (e.g., a birth defect of the stomach), and/or provide drainage/decompression of the stomach when it is necessary to bypass an obstruction of the stomach outlet into the small intestine. Although noninvasive disposable enteral feeding components may be included, surgical instruments and pharmaceutical agents are not included. This is a single-use device.
Who makes Moss?
Moss is made by Moss Tubes, Inc.. It is listed under gastrostomy and gj tubes in our device library.
What sizes does Moss come in?
Sizes listed for Moss: Catheter Gauge: 18 Fr. Confirm availability with the manufacturer's instructions for use.
Is Moss MRI safe?
The FDA device database entry for Moss does not state its MRI safety status. Check the labeling before MRI.
Is Moss FDA cleared?
Moss is covered by FDA submission K990389.
How do I contact a Moss Tubes, Inc. sales representative?
Moss Tubes, Inc. has not listed representatives on LA Vascular yet. Visit the Moss Tubes, 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.