mild Device Kit MDK-0001

GUDID B235MDK00010

VERTOS MEDICAL, INC.

Neurosurgical procedure kit, non-medicated, single-use

• Primary Device ID: B235MDK00010
• NIH Device Record Key: 2fb5b867-5afd-4d9e-866a-c35ba13d1347
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: mild Device Kit
• Version Model Number: MDK-0001
• Catalog Number: MDK-0001
• Company DUNS: 011925561
• Company Name: VERTOS MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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

Customer Support Contacts

• Phone: 8779586227
• Email: customerservice@vertosmed.com
• Phone: 8779586227
• Email: customerservice@vertosmed.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B235MDK00010 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-23

On-Brand Devices [mild Device Kit]

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