Accu-Line® 32-467618

GUDID 00887868560989

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00887868560989
• NIH Device Record Key: 337748f2-c395-4e9d-8eb4-1533a4542ac2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Accu-Line®
• Version Model Number: 32-467618
• Catalog Number: 32-467618
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868560989 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

[00887868560989]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-01
• Device Publish Date: 2023-07-24

On-Brand Devices [Accu-Line®]

• 00880304339965: 32-467619
• 00887868485961: 32-467249
• 00887868561009: 32-467619
• 00887868560989: 32-467618