Lulu Water Based Lubricant

GUDID 00850017860025

MANO & MANO PTY. LTD.

Sexual lubricant

• Primary Device ID: 00850017860025
• NIH Device Record Key: 88cc52d4-af0b-4f31-afe7-192714496248
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lulu Water Based Lubricant
• Version Model Number: 16 fl oz (500ml)
• Company DUNS: 749841222
• Company Name: MANO & MANO PTY. 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850017860025 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161585

FDA Product Code

• NUC: Lubricant, Personal

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: 2020-08-07
• Device Publish Date: 2020-06-01

On-Brand Devices [Lulu Water Based Lubricant ]

• 00850017860025: 16 fl oz (500ml)
• 00850017860148: 8 fl oz (250ml)