Silicone Penrose Straight Drain Tube

GUDID 04710961934752

FORTUNE MEDICAL INSTRUMENT CORP.

Surgical capillary wound drain, luminal, synthetic polymer

• Primary Device ID: 04710961934752
• NIH Device Record Key: 1f071276-759a-4b2a-815d-bd8974eba3bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Silicone Penrose Straight Drain Tube
• Version Model Number: 2011-0020
• 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	04710961934752 [Unit of Use]
GS1	14710961934759 [Primary]

FDA Product Code

• GBP: Catheter, Multiple Lumen

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: 2021-11-30
• Device Publish Date: 2021-11-22

On-Brand Devices [Silicone Penrose Straight Drain Tube]

• 04710961934752: 2011-0020
• 04710961934783: 2011-0045
• 04710961934776: 2011-0035
• 04710961934769: 2011-0025