Silicone Katheter voor Zelf-Katherisatie (Type Man-L) (UDI 04542187220681)
Manufactured by CREATE MEDIC CO., LTD.
Device Regulatory Overview
The Silicone Katheter voor Zelf-Katherisatie (Type Man-L) (Model/Catalog Number: 8000015799H) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification U010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8000015799H
- Product Code / EMDN
- U010199
- Device Name
- Self-Catheterization Set
- Database Sync Date
- 2026-08-09 16:30:32
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 Katheter voor Zelf-Katherisatie (Type Man-L)?
The registered manufacturer of record for Silicone Katheter voor Zelf-Katherisatie (Type Man-L) is CREATE MEDIC CO., LTD..
What is the Primary UDI-DI identifier for Silicone Katheter voor Zelf-Katherisatie (Type Man-L)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187220681.
What classification code is assigned to this device?
This device is registered under product classification code U010199.
Similar Classification Devices (U010199)
Other Devices by CREATE MEDIC CO., LTD.
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