K-Wire Depth Gauge 110018535

GUDID 00887868467240

Biomet Orthopedics, LLC

Surgical depth gauge, reusable

• Primary Device ID: 00887868467240
• NIH Device Record Key: efb60810-98c4-4cfa-975b-50986c6e5843
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-Wire Depth Gauge
• Version Model Number: 110018535
• Catalog Number: 110018535
• 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
• 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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868467240 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142658

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

[00887868467240]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-12
• Device Publish Date: 2021-04-02

On-Brand Devices [K-Wire Depth Gauge]

• 00887868024467: 2141-40-000
• 00887868002274: 14232
• 00887868001710: 13545
• 00887868049422: 8241-98-000
• 00887868458231: 13545
• 00887868467240: 110018535