DEPTH GAUGE W/ COUNTERSINK 110008461

GUDID 00887868109690

Biomet Orthopedics, LLC

Surgical depth gauge, reusable

• Primary Device ID: 00887868109690
• NIH Device Record Key: 3f837a23-2c40-4bc4-b9e8-f26dbf1ab9bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DEPTH GAUGE W/ COUNTERSINK
• Version Model Number: 110008461
• Catalog Number: 110008461
• 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)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868109690 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140891

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00887868109690]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-12-07
• Device Publish Date: 2016-09-26

On-Brand Devices [DEPTH GAUGE W/ COUNTERSINK]

• 00887868109706: 110008465
• 00887868109690: 110008461
• 00887868109683: 110008459
• 00887868463228: 110008465
• 00887868463204: 110008461
• 00887868463198: 110008459