Silicone Round Drain Kit

GUDID 04710961935728

FORTUNE MEDICAL INSTRUMENT CORP.

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• Primary Device ID: 04710961935728
• NIH Device Record Key: cc224c47-def9-45b3-9d12-c92aa78e3d50
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Round Drain Kit
• Version Model Number: 2015-9308
• 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	04710961935728 [Unit of Use]
GS1	14710961935725 [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 Kit]

• 04711182607449: 2015-9314
• 04710961935766: 2015-9320
• 04710961935759: 2015-9318
• 04710961935742: 2015-9316
• 04710961935735: 2015-9310
• 04710961935728: 2015-9308
• 04710961935667: 2015-9220
• 04710961935650: 2015-9218
• 04710961935643: 2015-9216
• 04710961935636: 2015-9214
• 04710961935629: 2015-9210
• 04710961935612: 2015-9208