Probe 901010

GUDID 00887868567469

Biomet Orthopedics, LLC

Endoscopic surgical probe

• Primary Device ID: 00887868567469
• NIH Device Record Key: a8ef3520-f77e-448b-89ec-9b0ae6ca6b43
• 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: 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
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868567469 [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

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

[00887868567469]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-06
• Device Publish Date: 2023-05-29

On-Brand Devices [Probe]

• 00880304402003: 901010
• 00887868567469: 901010