Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

MASON TAYLER MEDICAL

US

Last updated May 30, 2026

What MASON TAYLER MEDICAL makes

Mason Taylor Medical produces disposable gastric lavage kits designed for the removal of stomach contents, including the Gastric Lavage Kit, as well as variants featuring 36 Fr. and 32 Fr. lavage tubes. These kits are intended for clinical use in emergency or procedural settings to clear the gastrointestinal tract of fluids or foreign materials.

The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Mason Taylor Medical manufacture?

Mason Taylor Medical specializes in disposable gastric lavage kits. These devices are designed for clinical use to remove stomach contents, such as fluids or foreign materials, during emergencies or procedures. Examples include the standard Gastric Lavage Kit, as well as variants that include lavage tubes of different sizes, like 36 Fr. and 32 Fr.

Where is Mason Taylor Medical based?

Mason Taylor Medical is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

How are Mason Taylor Medical’s devices classified under FDA regulations?

Mason Taylor Medical’s gastric lavage kits are classified as Class II medical devices by the FDA. This classification applies to devices that generally pose moderate risk and require special controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.

Are Mason Taylor Medical’s devices listed in any regulatory registries?

Yes, Mason Taylor Medical’s devices are listed in the FDA Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their distribution and use, ensuring transparency and regulatory compliance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
888-270-7494
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
176382489

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Gastric Lavage Kit MTM5200
FDA UDI
Class IIActive
Gastric Lavage Kit with 36 Fr. Lavage Tube MTM5136
FDA UDI
Class IIActive
Gastric Lavage Kit with 32 Fr. Lavage Tube MTM5132
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.