OptiPLUS

GUDID 08052049500272

BIOS SRL

Radio-frequency skin contouring system

• Primary Device ID: 08052049500272
• NIH Device Record Key: 49150eb3-ad4f-4ab7-8243-4ff1298eab25
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OptiPLUS
• Version Model Number: APMD145-1ch.US-OptiPLUS
• Company DUNS: 443571203
• Company Name: BIOS SRL
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08052049500272 [Primary]

FDA Product Code

• PBX: Massager, Vacuum, Radio Frequency Induced Heat

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: 2023-08-31
• Device Publish Date: 2023-08-23

On-Brand Devices [OptiPLUS]

• 08052049500272: APMD145-1ch.US-OptiPLUS
• 08052049500289: APMD145-1ch.US-OptiPLUS