REVAREE

GUDID 08032595871064

FARMA DERMA SRL

Vaginal mucosa protection suppository

• Primary Device ID: 08032595871064
• NIH Device Record Key: 807d4b01-84c8-4ee8-95c7-f046b89d0e63
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REVAREE
• Version Model Number: VAGINAL SUPPOSITORIES 2 g
• Company DUNS: 541677746
• Company Name: FARMA DERMA SRL
• Device Count: 10
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08032595871064 [Primary]
GS1	08032595871088 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153372

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: 4
• Public Version Date: 2020-08-20
• Device Publish Date: 2018-02-26

On-Brand Devices [REVAREE ]

• 08032595871071: VAGINAL SUPPOSITORIES 2 g
• 08032595871064: VAGINAL SUPPOSITORIES 2 g