Silicone Round Drain

GUDID 04710961935568

FORTUNE MEDICAL INSTRUMENT CORP.

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• Primary Device ID: 04710961935568
• NIH Device Record Key: 36291dc4-ab80-440f-8ba1-b977c03ad650
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Round Drain
• Version Model Number: 2015-0210
• 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	04710961935568 [Unit of Use]
GS1	14710961935565 [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 Round Drain]

• 04711182607395: 2015-0314
• 04711182607388: 2015-0312
• 04711182607371: 2015-0212
• 04710961935711: 2015-0320
• 04710961935704: 2015-0318
• 04710961935698: 2015-0316
• 04710961935681: 2015-0310
• 04710961935674: 2015-0308
• 04710961935605: 2015-0220
• 04710961935599: 2015-0218
• 04710961935582: 2015-0216
• 04710961935575: 2015-0214
• 04710961935568: 2015-0210
• 04710961935551: 2015-0208