Silicone Flat Drain Kit

GUDID 04710961935032

FORTUNE MEDICAL INSTRUMENT CORP.

Closed-wound drain

• Primary Device ID: 04710961935032
• NIH Device Record Key: 1da19b62-16ea-468e-8cc4-d7e3d76a9e8b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Flat Drain Kit
• Version Model Number: 2014-9051
• 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	04710961935032 [Unit of Use]
GS1	14710961935039 [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 Flat Drain Kit]

• 04710961935100: 2014-9132
• 04710961935094: 2014-9131
• 04710961935087: 2014-9102
• 04710961935070: 2014-9101
• 04710961935063: 2014-9072
• 04710961935056: 2014-9071
• 04710961935049: 2014-9052
• 04710961935032: 2014-9051