Safire™ Blu™ SP A402869

GUDID 05414734310734

Ablation Catheter

IRVINE BIOMEDICAL, INC.

Cardiac radio-frequency ablation system catheter

• Primary Device ID: 05414734310734
• NIH Device Record Key: 209efa97-830e-4577-bc93-7ca44a13469e
• Commercial Distribution Discontinuation: 2020-04-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Safire™ Blu™ SP
• Version Model Number: A402869
• Catalog Number: A402869
• Company DUNS: 926346966
• Company Name: IRVINE BIOMEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: +1(855)478-5833
• Email: customerservice@sjm.com

Device Dimensions

• Catheter Gauge: 7 French

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry location

Device Identifiers

Device Issuing Agency	Device ID
GS1	05414734310734 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P060019

FDA Product Code

• OAD: catheter, percutaneous, cardiac ablation, for treatment of atrial flutter

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: 2020-05-01
• Device Publish Date: 2014-09-29

On-Brand Devices [Safire™ Blu™ SP]

• 05414734310765: Ablation Catheter
• 05414734310758: Ablation Catheter
• 05414734310741: Ablation Catheter
• 05414734310734: Ablation Catheter