Sofia DA6115ST

GUDID 00842429108444

Sofia 6F-115cm STR

MICROVENTION INC.

Vascular guide-catheter, single-use

• Primary Device ID: 00842429108444
• NIH Device Record Key: 4a337c16-559d-4d10-b0e5-b991856c1a11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sofia
• Version Model Number: DA6115ST-GC-OD
• Catalog Number: DA6115ST
• Company DUNS: 003263105
• Company Name: MICROVENTION INC.
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com
• Phone: +1(888) 775-0182
• Email: customerservice@microvention.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry. Keep away from sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842429108444 [Primary]

FDA Product Code

• DQO: Catheter, intravascular, diagnostic

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: 2024-10-28
• Device Publish Date: 2024-10-18

On-Brand Devices [Sofia]

• 00842429108482: Sofia 6F-131cm STR
• 00842429108475: Sofia 6F-125cm STR
• 00842429108468: Sofia 6F-131cm STR
• 00842429108451: Sofia 6F-125cm STR
• 00842429108444: Sofia 6F-115cm STR