Integral®

GUDID 00889024011373

ZIMMER DENTAL INC.

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00889024011373
• NIH Device Record Key: a5aa56c0-5548-48a2-a117-80c273e41cfc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Integral®
• Version Model Number: 0837
• 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	00889024011373 [Primary]

FDA Product Code

• NDP: ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

Moist Heat or Steam Sterilization

[00889024011373]

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 [Integral®]

• 00889024011434: 0949
• 00889024011427: 0948
• 00889024010918: 0426
• 00889024010901: 0422
• 00889024010956: 0494
• 00889024011465: 0999
• 00889024011403: 0936
• 00889024011373: 0837
• 00889024011359: 0815
• 00889024011151: 0701
• 00889024010925: 0431