Silicone Penrose Drain Tube (UDI 2010-6412)
Manufactured by FORTUNE MEDICAL INSTRUMENT CORP.
Device Regulatory Overview
The Silicone Penrose Drain Tube (Model/Catalog Number: 2010-6412) is a medical device manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. This product is indexed under FDA Product Code / Category Classification GCD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2010-6412
- Product Code / EMDN
- GCD
- Device Name
- Database Sync Date
- 2026-08-09 09:29:18
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Silicone Penrose Drain Tube?
The registered manufacturer of record for Silicone Penrose Drain Tube is FORTUNE MEDICAL INSTRUMENT CORP..
What is the Primary UDI-DI identifier for Silicone Penrose Drain Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2010-6412.
What classification code is assigned to this device?
This device is registered under product classification code GCD.
Similar Classification Devices (GCD)
Other Devices by FORTUNE MEDICAL INSTRUMENT CORP.
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