Silicone Hubless Endo Drain Kit

GUDID 04711182606107

FORTUNE MEDICAL INSTRUMENT CORP.

Closed-wound drain

• Primary Device ID: 04711182606107
• NIH Device Record Key: 00bccf3a-5eb9-4430-9cc0-37018845108e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Hubless Endo Drain Kit
• Version Model Number: 2015-9710
• 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	04711182606107 [Unit of Use]
GS1	14711182606104 [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 Kit]

• 04711182606145: 2015-9721
• 04711182606121: 2015-9719
• 04711182606114: 2015-9715
• 04711182606107: 2015-9710