JOVS Hair Removal Device

GUDID 06973698659772

Shenzhen Qianyu Technology Co., Ltd

Intense pulsed light skin surface treatment system

• Primary Device ID: 06973698659772
• NIH Device Record Key: fe5b78ad-58c7-4e18-bf21-ff319d07c55c
• Commercial Distribution Discontinuation: 2022-09-09
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: JOVS Hair Removal Device
• Version Model Number: JR5-E
• Company DUNS: 417324184
• Company Name: Shenzhen Qianyu Technology Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	06973698659772 [Primary]

FDA Product Code

• OHT: Light Based Over-The-Counter Hair Removal

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: 2022-09-16
• Device Publish Date: 2022-09-08

On-Brand Devices [JOVS Hair Removal Device]

• 06973698659895: JR5-E
• 06973698652247: JR5-OG
• 06973698652230: JR5-W
• 06973698650854: JR5C-OG
• 06973698650830: JR5C-W
• 06973698650823: JR5C-E
• 06973698659772: JR5-E
• 06973698659116: JR5C-OG
• 06973698659109: JR5C-W
• 06973698652339: JR5C-E