arboleaf

GUDID 06928081772651

Shenzhen Yolanda Technology Co.,Ltd.

Hand-held electric massager

• Primary Device ID: 06928081772651
• NIH Device Record Key: 87e48cd6-8dbc-466c-b2df-13309a4b2001
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: arboleaf
• Version Model Number: CM20F
• Company DUNS: 421347580
• Company Name: Shenzhen Yolanda 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: 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	06928081772651 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2025-05-01
• Device Publish Date: 2025-04-23

On-Brand Devices [arboleaf]

• 16928081771293: CS20W
• 16928081771255: SP10A
• 16928081771361: CS20M
• 06928081772422: SP20B
• 16928081771378: CS20N
• 06928081772651: CM20F
• 06928081771449: CM20C