mild Device Kit

GUDID 07613327651676

VERTOS MEDICAL, INC.

Orthopaedic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 07613327651676
• NIH Device Record Key: 5f3d4975-6e96-4c92-a797-f80bd0f83c14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: mild Device Kit
• Version Model Number: MDK-0002
• Company DUNS: 011925561
• Company Name: VERTOS MEDICAL, 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: true
• 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	07613327651676 [Primary]
HIBCC	B235MDK00020 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K233800

FDA Product Code

• HRX: Arthroscope

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: 2024-12-02
• Device Publish Date: 2024-11-22

On-Brand Devices [mild Device Kit]

• B235MDK00010: MDK-0001
• 07613327651683: MDK-0001
• 07613327651676: MDK-0002