Primocyn Eau Divine Skin Hydrogel 85035

GUDID 00860439002040

Sonoma Pharmaceuticals, Inc.

Wound hydrogel dressing, non-antimicrobial

• Primary Device ID: 00860439002040
• NIH Device Record Key: 6cce168c-db49-4bec-ac78-79e428b186db
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Primocyn Eau Divine Skin Hydrogel
• Version Model Number: 85035
• Catalog Number: 85035
• 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: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram
• Weight: 170 Gram

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860439002040 [Primary]
GS1	20860439002044 [Package]; Package: Box [12 Units]; In Commercial Distribution

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: 2022-12-12
• Device Publish Date: 2022-12-02

On-Brand Devices [Primocyn Eau Divine Skin Hydrogel]

• 00860439002040: 85035
• 00850015491214: 86004