PROBE 901010

GUDID 00880304402003

Biomet Orthopedics, LLC

Arthroscopic probe

• Primary Device ID: 00880304402003
• NIH Device Record Key: 2c8d4a5f-6f4a-4212-9f1b-d8d3dac6296b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROBE
• Version Model Number: 901010
• Catalog Number: 901010
• 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: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304402003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K933070

FDA Product Code

• HRX: Arthroscope

Sterilization

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

[00880304402003]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-07-28

On-Brand Devices [PROBE]

• 00880304402003: 901010
• 00887868567469: 901010