BP®

GUDID 00889024320703

ZIMMER SPINE, INC.

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• Primary Device ID: 00889024320703
• NIH Device Record Key: 7bac336e-6b05-4827-9a25-677a45eb7200
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BP®
• Version Model Number: 07.00008.031
• Company DUNS: 787663400
• Company Name: ZIMMER SPINE, INC.
• Device Count: 1
• 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(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com
• Phone: +1(866)774-6368
• Email: zimmer.consumerrelations@zimmer.com

Device Dimensions

• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter
• Length: 24 Millimeter
• Outer Diameter: 17 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024320703 [Primary]

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

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: 2020-02-24
• Device Publish Date: 2015-10-23

On-Brand Devices [BP®]

• 00889024320741: 07.00008.047
• 00889024320734: 07.00008.046
• 00889024320727: 07.00008.039
• 00889024320710: 07.00008.038
• 00889024320703: 07.00008.031
• 00889024320697: 07.00008.030
• 00889024320680: 07.00008.023
• 00889024320673: 07.00008.022
• 00889024320666: 07.00008.015
• 00889024320659: 07.00008.014
• 00889024320642: 07.00008.007
• 00889024338579: 8002-1724-00
• 00889024338562: 8002-1720-00
• 00889024338555: 8002-1524-00
• 00889024338548: 8002-1520-00