Removalon

GUDID 00348783003864

REMOVALON I DRY PK CASEOF 6

PREMIER DENTAL PRODUCTS COMPANY

Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent Medical device disinfection agent

• Primary Device ID: 00348783003864
• NIH Device Record Key: d63861e0-ff65-4b93-89b3-3dc18fef36e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Removalon
• Version Model Number: 9011005
• Company DUNS: 014789663
• Company Name: PREMIER DENTAL PRODUCTS COMPANY
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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	00348783003864 [Primary]

FDA Product Code

• FLG: Cleaner, Ultrasonic, Medical Instrument

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-06-28
• Device Publish Date: 2022-06-29

On-Brand Devices [Removalon]

• D6919011005: REMOVALON I DRY PK CASEOF 6
• D6918101998: REMOVALON I DRY PK SINGLE
• 00348783003864: REMOVALON I DRY PK CASEOF 6
• 00348783003857: REMOVALON I DRY PK SINGLE