EASEZEN

GUDID 06950940802186

Shenzhen Osto Technology Co.,Ltd.

Acupuncture electrical stimulation system

• Primary Device ID: 06950940802186
• NIH Device Record Key: e4f9a2d2-9371-4dba-8957-638ebf35be1c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EASEZEN
• Version Model Number: AST-300V
• Company DUNS: 528161684
• Company Name: Shenzhen Osto Technology Co.,Ltd.
• Device Count: 505
• 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06950940802179 [Primary]
GS1	06950940802186 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211736

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

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: 2024-09-09
• Device Publish Date: 2024-08-30

Devices Manufactured by Shenzhen Osto Technology Co.,Ltd.

• 06950940802230 - Be-Younger: 2024-11-19
• 06950940802254 - Be-Younger: 2024-11-19
• 06950940802216 - N/A: 2024-10-29
• 06950940802070 - N/A: 2024-09-09
• 06950940802094 - N/A: 2024-09-09
• 06950940802186 - EASEZEN: 2024-09-09
• 06950940802186 - EASEZEN: 2024-09-09
• 06950940802117 - VEVOR: 2024-08-28
• 06950940802131 - VEVOR: 2024-08-28