RAPIDFIRE® SYSTEM 15-1189

GUDID 00841036075002

BIOMET MICROFIXATION, INC

Surgical instrument/implant rack

• Primary Device ID: 00841036075002
• NIH Device Record Key: 3b5fce26-38f8-443c-b903-49490d48395a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAPIDFIRE® SYSTEM
• Version Model Number: 15-1189
• Catalog Number: 15-1189
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, 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: 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036075002 [Primary]

FDA Product Code

• LRP: TRAY, SURGICAL

Sterilization

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

[00841036075002]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-09-28
• Device Publish Date: 2018-08-28

On-Brand Devices [RAPIDFIRE® SYSTEM]

• 00841036080419: 91-6604
• 00841036075002: 15-1189