Ulti-Flo General Purpose Drainage Catheter LBNL-2050H

GUDID H862LBNL2050H2

HYDROPHILIC COATED LARGE BORE NON-LOCKING CATHETER, 20F

URESIL, LLC

Suction system catheter, general-purpose

• Primary Device ID: H862LBNL2050H2
• NIH Device Record Key: 38fa76ae-6ad0-4d7f-959b-a0bd5827c00b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ulti-Flo General Purpose Drainage Catheter
• Version Model Number: LBNL-2050H
• Catalog Number: LBNL-2050H
• Company DUNS: 192559557
• Company Name: URESIL, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-538-7374
• Email: uresil@sales.com

Device Dimensions

• Length: 41 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H862LBNL2050H0 [Primary]
HIBCC	H862LBNL2050H1 [Package]; Contains: H862LBNL2050H0; Package: Dipsenser [5 Units]; In Commercial Distribution
HIBCC	H862LBNL2050H2 [Package]; Contains: H862LBNL2050H1; Package: Shipper [4 Units]; In Commercial Distribution

FDA Product Code

• GBO: Catheter, Nephrostomy, General & Plastic Surgery

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-03-26
• Device Publish Date: 2016-08-29

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