WINK SLIDER

GUDID 00028373150245

WINK Slider Condom (24ct box)

OKAMOTO USA, INC.

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• Primary Device ID: 00028373150245
• NIH Device Record Key: 802bb527-81a7-4831-b313-b5545e72d2a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WINK SLIDER
• Version Model Number: 15024
• Company DUNS: 175752724
• Company Name: OKAMOTO USA, INC.
• Device Count: 24
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00028373150245 [Primary]
GS1	80028373150241 [Unit of Use]

FDA Product Code

• HIS: Condom

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-07-25
• Device Publish Date: 2019-10-04

On-Brand Devices [WINK SLIDER]

• 00028373150245: WINK Slider Condom (24ct box)
• 00028373150108: WINK Slider Condom (10ct box)
• 00028373150030: WINK Slider Condom (3ct box)