VANCOR

GUDID 08809342217228

ILSEONG Co., Ltd.

Pneumatic massager

• Primary Device ID: 08809342217228
• NIH Device Record Key: 8978bb81-2878-4c05-b494-057c087095c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VANCOR
• Version Model Number: LILIHEAL MASSAGE DEVICE
• Company DUNS: 694086812
• Company Name: ILSEONG 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: 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	08809342217228 [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: 2025-06-25
• Device Publish Date: 2025-06-17