Spline® Twist™ Implant System

GUDID 00889024013124

ZIMMER DENTAL INC.

Screw endosteal dental implant, two-piece

• Primary Device ID: 00889024013124
• NIH Device Record Key: 0ccf42be-118e-4d79-a336-f91ed161edcd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spline® Twist™ Implant System
• Version Model Number: 1989
• Company DUNS: 103167086
• Company Name: ZIMMER DENTAL INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(800)854-7019
• Email: zimmer.consumerrelations@zimmer.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024013124 [Primary]

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-10-21

On-Brand Devices [Spline® Twist™ Implant System]

• 00889024013315: 2135
• 00889024013308: 2133
• 00889024013292: 2131
• 00889024013285: 2130
• 00889024013278: 2121
• 00889024013261: 2120
• 00889024013193: 1996
• 00889024013186: 1995
• 00889024013179: 1994
• 00889024013162: 1993
• 00889024013155: 1992
• 00889024013148: 1991
• 00889024013131: 1990
• 00889024013124: 1989
• 00889024013117: 1988
• 00889024013100: 1987
• 00889024013094: 1986
• 00889024013087: 1985
• 00889024013070: 1984
• 00889024013063: 1983
• 00889024013056: 1982
• 00889024013049: 1981
• 00889024013032: 1980
• 00889024013025: 1979
• 00889024013018: 1961
• 00889024013001: 1960