HydroMID Catheter MID-141CM

GUDID 00850030354365

Midline 4Fr Single Lumen Marked Catheter

ACCESS VASCULAR, INC.

Peripherally-inserted central venous catheter

• Primary Device ID: 00850030354365
• NIH Device Record Key: af69953c-0d23-40e6-ac9d-7ae18d455e8a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HydroMID Catheter
• Version Model Number: MID-141CM
• Catalog Number: MID-141CM
• Company DUNS: 085539114
• Company Name: ACCESS VASCULAR, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850030354365 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220772

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: 2023-12-08
• Device Publish Date: 2023-11-30

Devices Manufactured by ACCESS VASCULAR, INC.

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