Silicone Vac-Drain

GUDID 04710961935360

FORTUNE MEDICAL INSTRUMENT CORP.

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• Primary Device ID: 04710961935360
• NIH Device Record Key: 80d0f322-b9d6-4933-8376-8782da4cfc09
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Vac-Drain
• Version Model Number: 2014-0421
• 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	04710961935360 [Unit of Use]
GS1	14710961935367 [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: 2022-02-08
• Device Publish Date: 2022-01-31

On-Brand Devices [Silicone Vac-Drain]

• 04710961935360: 2014-0421
• 04710961935353: 2014-0419
• 04710961935346: 2014-0415
• 04710961935339: 2014-0411
• 04710961935322: 2014-0410
• 04710961935315: 2014-0408