Omniloc™

GUDID 00889024011113

ZIMMER DENTAL INC.

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00889024011113
• NIH Device Record Key: 2235f8ba-e0fe-4208-9ab8-91e52fea8ec6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Omniloc™
• Version Model Number: 0684
• Company DUNS: 103167086
• Company Name: ZIMMER DENTAL INC.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00889024011113 [Primary]

FDA Product Code

• NDP: ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

[00889024011113]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-12-07
• Device Publish Date: 2017-02-10

On-Brand Devices [Omniloc™]

• 00889024011137: 0696
• 00889024011045: 0616
• 00889024011144: 0699
• 00889024011120: 0685
• 00889024011113: 0684
• 00889024011014: 0599