Voguestrap

GUDID 04719872850076

BONASSE ENTERPRISES CO., LTD.

Contact lens case

• Primary Device ID: 04719872850076
• NIH Device Record Key: c057fab1-4ce8-49b1-8707-42c97321cc93
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Voguestrap
• Version Model Number: SC-213
• Company DUNS: 657544912
• Company Name: BONASSE ENTERPRISES 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: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719872850076 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K991206

FDA Product Code

• LRX: Case, Contact Lens

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-06-29

On-Brand Devices [Voguestrap ]

• 04719872850137: SC-506
• 04719872850113: SC-503
• 04719872850076: SC-213