Zimmer® DTO®

GUDID 00889024487741

Zimmer GmbH

Spinal dynamic-stabilization system

• Primary Device ID: 00889024487741
• NIH Device Record Key: 88bb782e-3c06-4162-9ad1-83fedccef8d3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zimmer® DTO®
• Version Model Number: 01.03791.090
• Company DUNS: 488133448
• Company Name: Zimmer GmbH
• Device Count: 2
• DM Exempt: false
• 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)348-2759
• Email: zimmer.consumerrelations@zimmer.com

Device Dimensions

• Length: 90 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024407190 [Unit of Use]
GS1	00889024487741 [Primary]

FDA Product Code

• NQP: POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION

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: 2017-07-28

On-Brand Devices [Zimmer® DTO®]

• 00889024487741: 01.03791.090
• 00889024487734: 01.03791.070
• 00889024485051: 01.03791.080
• 00889024485044: 01.03791.060
• 00889024485037: 01.03791.050
• 00889024485020: 01.03791.040
• 00889024485013: 01.03791.100
• 00889024284456: Zimmer® DTO® Pin press
• 00889024284180: Zimmer DTO Implant 100
• 00889024284173: Zimmer DTO Implant 90
• 00889024284166: Zimmer DTO Implant 80
• 00889024284159: Zimmer DTO Implant 70
• 00889024284142: Zimmer DTO Implant 60
• 00889024284135: Zimmer DTO Implant 50
• 00889024284128: Zimmer DTO Implant 40