Set 8810000

GUDID DO3688100001

SDI LIMITED

Dental composite resin

• Primary Device ID: DO3688100001
• NIH Device Record Key: 79f2e130-ef45-4384-a34e-00a7cccd34bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Set
• Version Model Number: SET ASSORTED KT
• Catalog Number: 8810000
• Company DUNS: 753221852
• Company Name: SDI LIMITED
• Device Count: 50
• 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: true
• 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: +18002285166
• Email: info@sdi.com.au

Operating and Storage Conditions

• Handling Environment Atmospheric Pressure: Between 5 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	DO3688100000 [Unit of Use]
HIBCC	DO3688100001 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051008

FDA Product Code

• EMA: CEMENT, DENTAL

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: 2018-07-06
• Device Publish Date: 2016-10-10

On-Brand Devices [Set]

• DO3688100001: SET ASSORTED KT
• DO3688050031: SET OA3 50 CAP
• DO3688050021: SET A2 50 CAP
• DO3688050011: SET A1 50 CAP