Pulse Aloe-ahh

GUDID 00867003000211

Silicone based personal lubricant

TOASTER LABS, INC.

Sexual lubricant

• Primary Device ID: 00867003000211
• NIH Device Record Key: 83153f63-9c39-42a2-8194-e9121dfdae2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pulse Aloe-ahh
• Version Model Number: 1
• Company DUNS: 079882181
• Company Name: TOASTER LABS, INC.
• 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: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00867003000211 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152671

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: 5
• Public Version Date: 2018-08-14
• Device Publish Date: 2017-01-03

Devices Manufactured by TOASTER LABS, INC.

• 00867003000204 - Pulse H2Oh!: 2018-08-14 Water based personal lubricant
• 00867003000211 - Pulse Aloe-ahh: 2018-08-14Silicone based personal lubricant
• 00867003000211 - Pulse Aloe-ahh: 2018-08-14 Silicone based personal lubricant