ONPOINT 24-3200

GUDID 00841036130244

BIOMET MICROFIXATION, INC

Endoscopic video imaging system

• Primary Device ID: 00841036130244
• NIH Device Record Key: 5c60115a-5b62-4c7d-9d68-c6cc6cc292cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ONPOINT
• Version Model Number: 24-3200
• Catalog Number: 24-3200
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, INC
• 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036130244 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082293

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

[00841036130244]

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: 2015-10-11

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