Massage Gun

GUDID 06974581810225

Massager, Therapeutic, Electric

ShenZhen Pentasmart Technology Co,.Ltd

Hand-held electric massager

• Primary Device ID: 06974581810225
• NIH Device Record Key: dd05e477-6aa7-4727-8570-b8f95f435a61
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Massage Gun
• Version Model Number: uLax-6582A
• Company DUNS: 551250083
• Company Name: ShenZhen Pentasmart 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974581810225 [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: 2021-09-03
• Device Publish Date: 2021-08-26

On-Brand Devices [Massage Gun]

• 06974581810065: Massager, Therapeutic, Electric
• 06974581810225: Massager, Therapeutic, Electric