DRY RITE DRYING AGENT

GUDID D701SDRY12

1 oz bottle with dropper spout

PULPDENT CORPORATION

Medical device cleaning agent

• Primary Device ID: D701SDRY12
• NIH Device Record Key: ad8e8776-cb71-49d6-9807-1d2b335c42d6
• Commercial Distribution Discontinuation: 2019-01-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: DRY RITE DRYING AGENT
• Version Model Number: DRY1
• Company DUNS: 001006089
• Company Name: PULPDENT CORPORATION
• 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: true
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Total Volume: 1 Fluid Ounce

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D701SDRY12 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K896654

FDA Product Code

• EBF: Material, Tooth Shade, Resin

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-11-26
• Device Publish Date: 2018-08-10

Devices Manufactured by PULPDENT CORPORATION

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