K-WIRE DEPTH GAUGE 14232

GUDID 00887868002274

Biomet Orthopedics, LLC

Surgical depth gauge, reusable

• Primary Device ID: 00887868002274
• NIH Device Record Key: 260c7c42-823f-4c47-8876-0ee6f68033d1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-WIRE DEPTH GAUGE
• Version Model Number: 14232
• Catalog Number: 14232
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868002274 [Primary]

FDA Product Code

• HTJ: GAUGE, DEPTH

Sterilization

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

[00887868002274]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-12-07
• Device Publish Date: 2017-04-12

On-Brand Devices [K-WIRE DEPTH GAUGE]

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