LOCKING DRILL GUIDE 214207027

GUDID 00887868446504

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00887868446504
• NIH Device Record Key: 500dd787-178a-4982-9c7b-8a1b3cd34caa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOCKING DRILL GUIDE
• Version Model Number: 2142-07-027
• Catalog Number: 214207027
• 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

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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868446504 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

[00887868446504]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-14
• Device Publish Date: 2020-09-04

On-Brand Devices [LOCKING DRILL GUIDE]

• 00880304533554: 2312-00-109
• 00887868446504: 2142-07-027
• 00887868445736: 2142-07-020