Hydraview 901021-01

GUDID 00816349010439

BRIVANT LIMITED

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 00816349010439
• NIH Device Record Key: edfb3dd2-1841-4851-8a11-1114758e08a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hydraview
• Version Model Number: HVIEW GW, ES, S 190-014
• Catalog Number: 901021-01
• Company DUNS: 985303473
• Company Name: BRIVANT LIMITED
• 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	00816349010439 [Primary]

FDA Product Code

• DQX: Wire, Guide, Catheter

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: 2017-05-23

On-Brand Devices [Hydraview ]

• 00816349010484: HVIEW GW, EDS-J, J 190-014
• 00816349010477: HVIEW GW, DS-J, J 190-014
• 00816349010460: HVIEW GW, ES-J, J-TIP 190-014
• 00816349010453: HVIEW GW, EDS, S TIP 190-014
• 00816349010446: HVIEW GW, DS, S 190-014
• 00816349010439: HVIEW GW, ES, S 190-014