Knee massager

GUDID 06974581810188

Massager, Therapeutic, Electric, heated

ShenZhen Pentasmart Technology Co,.Ltd

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• Primary Device ID: 06974581810188
• NIH Device Record Key: 1eebd8c9-ffc9-49ab-86ce-dcaac72aeb11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Knee massager
• Version Model Number: uLap-6550B
• 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	06974581810188 [Primary]

FDA Product Code

• IRT: Pad, Heating, Powered

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: 2021-09-07
• Device Publish Date: 2021-08-30

On-Brand Devices [Knee massager]

• 06974581810027: Massager, Therapeutic, Electric
• 06974581810195: Massager, Therapeutic, Electric, heated
• 06974581810188: Massager, Therapeutic, Electric, heated