HydroMID

GUDID 00850030354174

HydroMID 5Fr Dual Lumen Marked catheter - Maximal Barrier kit

Access Vascular, Inc.

General surgical procedure kit, medicated

• Primary Device ID: 00850030354174
• NIH Device Record Key: 780160af-84c8-47af-9552-d235dac1a131
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HydroMID
• Version Model Number: 80H06104
• Company DUNS: 085539114
• Company Name: Access Vascular, 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850030354174 [Primary]

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: 2025-11-26
• Device Publish Date: 2025-11-18

On-Brand Devices [HydroMID]

• 00862559000449: Midline catheter
• 00850030354419: Marked Midline Catheter (Mobile Kit)
• 00850030354433: HydroMID 5Fr Dual Lumen Marked catheter - Mobile Maximal Barrier kit
• 00850030354426: HydroMID 5Fr Dual Lumen Marked catheter
• 00850030354174: HydroMID 5Fr Dual Lumen Marked catheter - Maximal Barrier kit
• 00850030354167: HydroMID 5Fr Dual Lumen Marked catheter - Basic kit