Cupping Device

GUDID 06974581810232

Massager, Therapeutic, Electric, heated

ShenZhen Pentasmart Technology Co,.Ltd

Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager

• Primary Device ID: 06974581810232
• NIH Device Record Key: 590fdabb-2495-400f-9817-caf76db859f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cupping Device
• Version Model Number: uCute-2500B
• 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	06974581810232 [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 [Cupping Device]

• 06974581810072: Device, Pressure Applying
• 06974581810256: Massager, Therapeutic, Electric, heated
• 06974581810232: Massager, Therapeutic, Electric, heated