Flagship SB 1702-006-010

GUDID 10816349010931

BRIVANT LIMITED

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 10816349010931
• NIH Device Record Key: 1783008c-2fe6-49e4-bb22-06876307389f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flagship SB
• Version Model Number: FSHP SB GPS, MED,J6,HY 195-014
• Catalog Number: 1702-006-010
• 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	00816349010934 [Primary]
GS1	10816349010931 [Package]; Contains: 00816349010934; Package: Inner Carton [5 Units]; In Commercial Distribution

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: 2017-05-05

On-Brand Devices [Flagship SB ]

• 10816349010948: FSHP SB GPS, J4, HY 195-014
• 10816349010931: FSHP SB GPS, MED,J6,HY 195-014
• 10816349010924: FSHP SB GPS,FLPY,J4,HY 195-014