IV Catheter

GUDID 10853620005187

Merit Pharmaceutical

Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter Peripheral vascular catheter

• Primary Device ID: 10853620005187
• NIH Device Record Key: 38d83f19-6789-45e6-ba14-7af78ed3f42c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IV Catheter
• Version Model Number: 035662588000
• Company DUNS: 093370369
• Company Name: Merit Pharmaceutical
• 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: 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: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com
• Phone: (323) 227-4831
• Email: solutions@meritpharm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853620005180 [Primary]
GS1	10853620005187 [Package]; Contains: 00853620005180; Package: [50 Units]; In Commercial Distribution
GS1	20853620005184 [Package]; Package: [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071382

FDA Product Code

• FOZ: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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: 2019-02-01
• Device Publish Date: 2019-01-01

On-Brand Devices [IV Catheter]

• 20853620005221: 035599853000
• 10853620005187: 035662588000