BE POD®

GUDID 03661489518232

FOURNITURES HOSPITALIERES INDUSTRIE

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 03661489518232
• NIH Device Record Key: 159b0f41-f10d-4f51-ab49-4cece678ec22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BE POD®
• Version Model Number: 251823 - CANNULATED ARTHRODESIS SCREW, L32
• Company DUNS: 261839898
• Company Name: FOURNITURES HOSPITALIERES INDUSTRIE
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03661489518232 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070617

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-02-19
• Device Publish Date: 2015-10-24

On-Brand Devices [BE POD®]

• 03661489518270: 251827 - CANNULATED ARTHRODESIS SCREW, L40
• 03661489518263: 251826 - CANNULATED ARTHRODESIS SCREW, L38
• 03661489518256: 251825 - CANNULATED ARTHRODESIS SCREW, L36
• 03661489518249: 251824 - CANNULATED ARTHRODESIS SCREW, L34
• 03661489518232: 251823 - CANNULATED ARTHRODESIS SCREW, L32
• 03661489518225: 251822 - CANNULATED ARTHRODESIS SCREW, L30
• 03661489518218: 251821 - CANNULATED ARTHRODESIS SCREW, L28TAPHYSIS