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PROACT MEDICAL LIMITED

US

Last updated May 27, 2026

Part of PROACT Medical Ltd.

What PROACT MEDICAL LIMITED makes

ProAct Medical Limited manufactures reusable laryngoscope blades designed for use in airway management procedures. Their primary product, the PROACT Smoothline LF, is engineered for clinical applications requiring precise visualization of the vocal cords and trachea during intubation.

The company’s laryngoscope blades are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) system. 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 ProAct Medical Limited manufacture?

ProAct Medical Limited specializes in reusable laryngoscope blades, which are used in airway management procedures. These devices are specifically designed to assist clinicians in visualizing the vocal cords and trachea during intubation, ensuring precise and effective airway control.

Where is ProAct Medical Limited based?

ProAct Medical Limited is headquartered in the United States. The company’s location is relevant for understanding regulatory oversight and compliance, particularly under FDA guidelines.

Which regulatory registries list ProAct Medical Limited’s devices?

ProAct Medical Limited’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency in the medical device supply chain, helping healthcare providers and regulators verify product details.

How are ProAct Medical Limited’s devices classified under FDA regulations?

ProAct Medical Limited’s laryngoscope blades fall under Class I classification according to FDA regulations. This classification is typically assigned to low-risk devices, though compliance with manufacturing and labeling requirements remains mandatory to maintain regulatory standing.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
+441536461981
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
491090502

Catalogue (14)

DeviceModel / ReferenceRegistriesClassStatus
PROACT Smoothline LF SLGS30MAC4
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MIL2
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30LT4
FDA UDI
Class IActive
PROACT Smoothline SLGS30MIL4
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30LT3
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MAC1
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MAC0
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MAC5
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MIL1
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MIL00
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MAC3
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MIL3
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MIL0
FDA UDI
Class IActive
PROACT Smoothline LF SLGS30MAC2
FDA UDI
Class IActive

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