Silicone Endo-Drain

GUDID 04710961935780

FORTUNE MEDICAL INSTRUMENT CORP.

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• Primary Device ID: 04710961935780
• NIH Device Record Key: b9e22790-6140-4d00-8696-44e7362c006f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Endo-Drain
• Version Model Number: 2015-0615
• Company DUNS: 656763489
• Company Name: FORTUNE MEDICAL INSTRUMENT CORP.
• Device Count: 10
• 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	04710961935780 [Unit of Use]
GS1	14710961935787 [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 Endo-Drain]

• 04711182605537: 2015-0629
• 04711182605520: 2015-0624
• 04710961935803: 2015-0621
• 04710961935797: 2015-0619
• 04710961935780: 2015-0615
• 04710961935773: 2015-0610