ReadiCath All Silicone Reusable Catheter Set ・Male L Type (UDI 04542187216455)
Manufactured by CREATE MEDIC CO., LTD.
Device Regulatory Overview
The ReadiCath All Silicone Reusable Catheter Set ・Male L Type (Model/Catalog Number: 8000015982H) 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
- 8000015982H
- Product Code / EMDN
- U010199
- Device Name
- Self-Catheterization Set
- Database Sync Date
- 2026-08-09 16:29:38
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 ReadiCath All Silicone Reusable Catheter Set ・Male L Type?
The registered manufacturer of record for ReadiCath All Silicone Reusable Catheter Set ・Male L Type is CREATE MEDIC CO., LTD..
What is the Primary UDI-DI identifier for ReadiCath All Silicone Reusable Catheter Set ・Male L Type?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187216455.
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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