AG PROFESSIONAL

GUDID 18809118711070

Hansol Medical Co.

Cupping therapy device

• Primary Device ID: 18809118711070
• NIH Device Record Key: 811cfaa4-02b7-4e94-8189-09949cfa80c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AG PROFESSIONAL
• Version Model Number: AG PROFESSIONAL CUPPING SET
• Company DUNS: 557793906
• Company Name: Hansol Medical Co.
• 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: false
• Manufacturing Date: false
• 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	08809118711073 [Primary]
GS1	18809118711070 [Package]; Contains: 08809118711073; Package: Carton box [10 Units]; In Commercial Distribution

FDA Product Code

• KNM: Device, Pressure Applying

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-23
• Device Publish Date: 2019-08-09

Devices Manufactured by Hansol Medical Co.

• 08809118710038 - Hansol Medical Co.: 2021-05-17
• 08809118710052 - Hansol Medical Co.: 2021-05-17
• 08809118710076 - Hansol Medical Co.: 2021-05-17
• 08809118710090 - Hansol Medical Co.: 2021-05-17
• 08809118710113 - Hansol Medical Co.: 2021-05-17
• 08809118710212 - Hansol Medical Co.: 2021-05-17
• 08809118710236 - Hansol Medical Co.: 2021-05-17
• 08809118710250 - Hansol Medical Co.: 2021-05-17