Cupping Device

GUDID 06974581810072

Device, Pressure Applying

ShenZhen Pentasmart Technology Co,.Ltd

Acupressure applicator, reusable Acupressure applicator, reusable Acupressure applicator, reusable Acupressure applicator, reusable Acupressure applicator, reusable Acupressure applicator, reusable Acupressure applicator, reusable Acupressure applicator, reusable

• Primary Device ID: 06974581810072
• NIH Device Record Key: c0228040-fbe3-43fc-8482-7a5290171885
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cupping Device
• Version Model Number: uCute-2500A
• 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	06974581810072 [Primary]

FDA Product Code

• KNM: Device, Pressure Applying

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: 2021-07-28
• Device Publish Date: 2021-07-20

On-Brand Devices [Cupping Device]

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