WINK

GUDID 00028373810101

WINK X-Large Condom (10ct box)

OKAMOTO USA, INC.

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• Primary Device ID: 00028373810101
• NIH Device Record Key: ecb98f8a-9fff-4e39-88b2-4d0e0a86f9a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WINK
• Version Model Number: 81010
• Company DUNS: 175752724
• Company Name: OKAMOTO USA, INC.
• Device Count: 10
• 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	00028373810101 [Primary]
GS1	80028373810107 [Unit of Use]

FDA Product Code

• HIS: Condom

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: 2019-11-11
• Device Publish Date: 2019-11-01

On-Brand Devices [WINK]

• 00028373810248: WINK X-Large Condom (24ct box)
• 00028373810101: WINK X-Large Condom (10ct box)
• 00028373810033: WINK X-Large Condom (3ct box)
• 00028373510247: WINK Studded Condom (24ct box)
• 00028373510100: WINK Studded Condom (10ct box)
• 00028373510032: WINK Studded Condom (3ct box)
• 00028373140017: WINK Closer Condom (1ct pack)