3i T3® SHORT DCD®

GUDID 00844868033592

3i T3® SHORT EXTERNAL HEX PARALLEL WALLED IMPLANT WITH DCD®, 5MM(D) X 5MM(L)

BIOMET 3I, LLC

Screw endosteal dental implant, two-piece

• Primary Device ID: 00844868033592
• NIH Device Record Key: 96ffb815-32e4-49a8-8cc6-8105ff45e9ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3i T3® SHORT DCD®
• Version Model Number: BNES505
• Company DUNS: 186127825
• Company Name: BIOMET 3I, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@biomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0
• Length: 5 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844868033592 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150571

FDA Product Code

• DZE: IMPLANT, ENDOSSEOUS, ROOT-FORM

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-12-01

On-Brand Devices [3i T3® SHORT DCD®]

• 00844868033622: 3i T3® SHORT EXTERNAL HEX PARALLEL WALLED IMPLANT WITH DCD®, 6MM(D) X 6MM(L)
• 00844868033615: 3i T3® SHORT EXTERNAL HEX PARALLEL WALLED IMPLANT WITH DCD®, 6MM(D) X 5MM(L)
• 00844868033608: 3i T3® SHORT EXTERNAL HEX PARALLEL WALLED IMPLANT WITH DCD®, 5MM(D) X 6MM(L)
• 00844868033592: 3i T3® SHORT EXTERNAL HEX PARALLEL WALLED IMPLANT WITH DCD®, 5MM(D) X 5MM(L)