Alliance SSI004730

GUDID 00889024518018

Zimmer, Inc.

Orthopaedic broach

• Primary Device ID: 00889024518018
• NIH Device Record Key: 2beb6a7c-9230-4d49-983c-4682aa81b5eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alliance
• Version Model Number: SSI004730
• Catalog Number: SSI004730
• Company DUNS: 056038268
• Company Name: Zimmer, 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: false
• Lot Batch: false
• Serial Number: true
• 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) 343-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024518018 [Primary]

FDA Product Code

• HTR: Rasp

Sterilization

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

[00889024518018]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-09-24
• Device Publish Date: 2018-08-23

On-Brand Devices [Alliance]

• 00889024518063: SSI004735
• 00889024518056: SSI004734
• 00889024518049: SSI004733
• 00889024518032: SSI004732
• 00889024518025: SSI004731
• 00889024518018: SSI004730
• 00889024518001: SSI004729
• 00889024517998: SSI004680
• 00889024517981: SSI004679
• 00889024517974: SSI004678
• 00889024682047: 110040476
• 00889024682030: 110040237
• 00889024682016: 110040439
• 00889024681996: 110040339
• 00889024681972: 110037010
• 00889024681927: 110040236
• 00889024681903: 110040444
• 00889024681897: 110040235