A+D Antimicrobial Hydrogel Spray 40930

GUDID 10365197409300

Sonoma Pharmaceuticals, Inc.

Wound hydrogel dressing, non-antimicrobial

• Primary Device ID: 10365197409300
• NIH Device Record Key: d34eca55-d209-4694-a07b-507ef27aa08a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A+D Antimicrobial Hydrogel Spray
• Version Model Number: 86042
• Catalog Number: 40930
• Company DUNS: 081642964
• Company Name: Sonoma Pharmaceuticals, 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: true
• 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 Dimensions

• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram
• Weight: 57 Gram

Device Identifiers

Device Issuing Agency	Device ID
GS1	00365197409303 [Primary]
GS1	10365197409300 [Package]; Contains: 00365197409303; Package: Box [120 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171935

FDA Product Code

• FRO: Dressing, Wound, Drug

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: 2025-06-18
• Device Publish Date: 2025-06-10

On-Brand Devices [A+D Antimicrobial Hydrogel Spray]

• 20365197409000: 86031
• 10365197409300: 86042