LOLA

GUDID 00851617007339

FORUM BRANDS, LLC

Basic male condom, Hevea-latex

• Primary Device ID: 00851617007339
• NIH Device Record Key: 31350754-deba-4829-8b66-c3545922cecb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOLA
• Version Model Number: 24ct Ultra Thin Lubricated Condoms
• Company DUNS: 055659749
• Company Name: FORUM BRANDS, LLC
• 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00850017666016 [Package]; Contains: 00851617007827; Package: Master Case [24 Units]; In Commercial Distribution
GS1	00851617007339 [Unit of Use]
GS1	00851617007827 [Primary]

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: 4
• Public Version Date: 2024-08-29
• Device Publish Date: 2020-06-30

On-Brand Devices [LOLA]

• 00851617007339: 24ct Ultra Thin Lubricated Condoms
• 10850038563155: FRMBR1-LZ3-CW3SX
• 10810092259388: FRMBR1-LZ3-C75SC
• 10850038563148: 8CT Super + Compact Applicator Tampons
• 10850038563131: 8CT Super Compact Applicator Tampons
• 10850033446965: 8CT Regular Compact Applicator Tampons
• 10850033446361: 8CT Light Compact Applicator Tampons
• 10810092259951: 8 CT SUPER+ NON-APPLICATOR TAMPONS
• 10810092259968: 8 CT SUPER NON-APPLICATOR TAMPONS