SELECT TEMPORARY CEMENT TUBE PKG EUGENOL 199-1063

GUDID D77819910630

SCOTT'S DENTAL SUPPLY L.L.C.

Zinc phosphate dental cement

• Primary Device ID: D77819910630
• NIH Device Record Key: 7e0fff70-17f7-40f5-b6c7-1d63aedc5779
• Commercial Distribution Discontinuation: 2018-09-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: SELECT TEMPORARY CEMENT TUBE PKG EUGENOL
• Version Model Number: 199-1063
• Catalog Number: 199-1063
• Company DUNS: 137217043
• Company Name: SCOTT'S DENTAL SUPPLY L.L.C.
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-901-3368
• Email: info@scottsdental.com
• Phone: 800-901-3368
• Email: info@scottsdental.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 10 Degrees Celsius and 24 Degrees Celsius
• Storage Environment Temperature: Between 10 Degrees Celsius and 24 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D77819910630 [Primary]

FDA Product Code

• EMB: Zinc Oxide Eugenol

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: 2018-12-04
• Device Publish Date: 2017-02-13