LiquID 071 M2000

GUDID 00850012180012

Guide Catheter Extension

Seigla Medlcal Inc.

Vascular guide-catheter extension

• Primary Device ID: 00850012180012
• NIH Device Record Key: ee2dbf1b-53b9-49cb-a543-fb8864b9bdc8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LiquID 071
• Version Model Number: 7F
• Catalog Number: M2000
• Company DUNS: 035365243
• Company Name: Seigla Medlcal 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

Device Dimensions

• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French
• Catheter Gauge: 7 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850012180012 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220691

FDA Product Code

• DQY: Catheter, Percutaneous

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: 2023-07-24
• Device Publish Date: 2023-07-14

On-Brand Devices [LiquID 071]

• 00850012180036: Guide Catheter Extension
• 00850012180012: Guide Catheter Extension