CROSSLOCK NARROW BLOCK LEFT SSI008303

GUDID 00889024700116

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00889024700116
• NIH Device Record Key: 06ad4a02-052b-42a4-956d-46e3f11cd727
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CROSSLOCK NARROW BLOCK LEFT
• Version Model Number: SSI008303
• Catalog Number: SSI008303
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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: 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 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.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 Identifiers

Device Issuing Agency	Device ID
GS1	00889024700116 [Primary]

FDA Product Code

• LXT: Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

Sterilization

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

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

[00889024700116]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-09
• Device Publish Date: 2025-12-01

Devices Manufactured by Biomet Orthopedics, LLC

• 70889024703154 - Threaded Tip Steinmann Pin: 2025-12-10
• 00889024703193 - Modular Arthrodesis Nail: 2025-12-10
• 00889024703209 - Modular Arthrodesis Nail: 2025-12-10
• 00889024703216 - Modular Arthrodesis Nail: 2025-12-10
• 00889024703230 - Modular Arthrodesis Nail: 2025-12-10
• 00889024703254 - Modular Arthrodesis Nail: 2025-12-10
• 00889024703261 - OSS™ Orthopedic Salvage System: 2025-12-10
• 00889024703285 - OSS™ Orthopedic Salvage System: 2025-12-10