VENAPAX XL

GUDID 00888233078986

BIOMET MICROFIXATION, INC

Flexible endoscopic scissors, reusable

• Primary Device ID: 00888233078986
• NIH Device Record Key: 8a832436-2109-41f2-ba31-00064f784d61
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VENAPAX XL
• Version Model Number: VPX4000
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888233078986 [Primary]
HIBCC	M718VPX4000 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140603

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-08
• Device Publish Date: 2025-03-31

Devices Manufactured by BIOMET MICROFIXATION, INC

• 00888233078986 - VENAPAX XL: 2025-04-08
• 00888233078986 - VENAPAX XL: 2025-04-08
• 00888233012430 - N/A: 2025-03-06
• 00888233013680 - CMF SYSTEM: 2025-03-06
• 00888233013703 - CMF SYSTEM: 2025-03-06
• 00888233013727 - CMF SYSTEM: 2025-03-06
• 00888233013741 - CMF SYSTEM: 2025-03-06
• 00888233025348 - LactoSorb System: 2025-03-06
• 00888233025355 - LactoSorb System: 2025-03-06