Silicone Hubless Endo-Drain Tube

GUDID 04711182606091

FORTUNE MEDICAL INSTRUMENT CORP.

Closed-wound drain

• Primary Device ID: 04711182606091
• NIH Device Record Key: db5ec366-ecfd-40dc-aa6c-4d8719121456
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Hubless Endo-Drain Tube
• Version Model Number: 2015-0729
• Company DUNS: 656763489
• Company Name: FORTUNE MEDICAL INSTRUMENT CORP.
• Device Count: 5
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04711182606091 [Unit of Use]
GS1	14711182606098 [Primary]

FDA Product Code

• GCD: Connector, Catheter

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: 2022-01-17
• Device Publish Date: 2022-01-07

On-Brand Devices [Silicone Hubless Endo-Drain Tube]

• 04711182606091: 2015-0729
• 04711182606084: 2015-0724
• 04711182606077: 2015-0721
• 04711182606053: 2015-0719
• 04711182606046: 2015-0715
• 04711182606039: 2015-0710