Silicone Vac-Drain Kit

GUDID 04710961935391

FORTUNE MEDICAL INSTRUMENT CORP.

Closed-wound drain

• Primary Device ID: 04710961935391
• NIH Device Record Key: baf07e39-c7ae-4229-8664-705472a86a8b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Vac-Drain Kit
• Version Model Number: 2014-9411
• 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	04710961935391 [Unit of Use]
GS1	14710961935398 [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 Kit]

• 04710961935421: 2014-9421
• 04710961935414: 2014-9419
• 04710961935407: 2014-9415
• 04710961935391: 2014-9411
• 04710961935384: 2014-9410
• 04710961935377: 2014-9408