PowerPulse Device

GUDID 06976287180992

Guangzhou Longest Medical Technology Co., Ltd.

Electromechanical orthopaedic extracorporeal shock wave therapy system

• Primary Device ID: 06976287180992
• NIH Device Record Key: 4760b1ac-899c-4949-8a63-b817f5d335e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PowerPulse Device
• Version Model Number: LGT-2520AP
• Company DUNS: 550274189
• Company Name: Guangzhou Longest Medical Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06976287180992 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-09-30
• Device Publish Date: 2024-09-20

Devices Manufactured by Guangzhou Longest Medical Technology Co., Ltd.

• 06976287180992 - PowerPulse Device: 2024-09-30
• 06976287180992 - PowerPulse Device: 2024-09-30
• 06976287181005 - Deep Oscillation Therapy Device: 2024-09-30
• 06976287180862 - Radial Pressure Pulse Therapy Device: 2024-07-30
• 06976287180879 - Radial Pressure Pulse Therapy Device: 2024-07-30
• 06976287180886 - Focused Shock Wave Therapy Device: 2024-07-30
• 06976287180466 - Radial Pressure Pulse Therapy Device: 2024-07-26
• 06976287180794 - Compression Therapy Device: 2024-07-26
• 06976287180800 - Portable Electro-Stimulation Therapy Device: 2024-07-26