NovaCross A02-108

GUDID 07290017436012

NITILOOP LTD

Vascular microcatheter

• Primary Device ID: 07290017436012
• NIH Device Record Key: 702b7306-6d50-4b22-8e31-edbed18b8510
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NovaCross
• Version Model Number: Xtreme
• Catalog Number: A02-108
• Company DUNS: 649175353
• Company Name: NITILOOP LTD
• 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: 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	07290017436012 [Primary]

FDA Product Code

• DQY: Catheter, Percutaneous

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: 2020-02-17
• Device Publish Date: 2020-02-09

Devices Manufactured by NITILOOP LTD

• 07290017436005 - NovaCross Microcatheter: 2020-04-14
• 07290017436012 - NovaCross: 2020-02-17
• 07290017436012 - NovaCross: 2020-02-17