GuruNanda

GUDID 00810051089004

GuruNanda Dry Mouth 33 oz

Gurunanda, LLC

Artificial saliva

• Primary Device ID: 00810051089004
• NIH Device Record Key: 3239bbf0-b413-460e-b609-a3712e3ca667
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GuruNanda
• Version Model Number: GNF135
• Company DUNS: 079671169
• Company Name: Gurunanda, LLC
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810051089004 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231205

FDA Product Code

• LFD: Saliva, Artificial

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: 2026-02-05
• Device Publish Date: 2026-01-28

On-Brand Devices [GuruNanda]

• 00810051084634: H3200
• 00810051089479: GuruNanda Dry Mouth 16 oz.
• 00810051089004: GuruNanda Dry Mouth 33 oz