Brainlab Flexible Catheter 19772

GUDID 04056481006426

Brainlab AG

Vascular microcatheter

• Primary Device ID: 04056481006426
• NIH Device Record Key: 4b481f7a-d342-4673-bd91-7f12f5525398
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Brainlab Flexible Catheter
• Version Model Number: 19772
• Catalog Number: 19772
• Company DUNS: 314482980
• Company Name: Brainlab AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49899915680
• Email: contact@brainlab.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056481006426 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123605

FDA Product Code

• HCA: Catheter, Ventricular

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: 2019-03-21
• Device Publish Date: 2016-09-15

On-Brand Devices [Brainlab Flexible Catheter]

• 04056481006440: 19770
• 04056481006433: 19771
• 04056481006426: 19772
• 04056481006419: 19773