PROVISIONAL FIXATION PIN LONG 824299001

GUDID 00887868049613

Biomet Orthopedics, LLC

Orthopaedic bone wire

• Primary Device ID: 00887868049613
• NIH Device Record Key: 42741ae8-3200-4f0e-b604-be2f4338b556
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROVISIONAL FIXATION PIN LONG
• Version Model Number: 8242-99-001
• Catalog Number: 824299001
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868049613 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00887868049613]

Moist Heat or Steam Sterilization

[00887868049613]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-28

On-Brand Devices [PROVISIONAL FIXATION PIN LONG]

• 00887868049613: 8242-99-001
• 00887868446658: 8242-99-001