Rektální rourka RIOCATH modrá (UDI 08593085011419)
Manufactured by Riocath Rectal Tube, a.s.
Device Regulatory Overview
The Rektální rourka RIOCATH modrá (Model/Catalog Number: 01.01.000.01.03) is a medical device manufactured by Riocath Rectal Tube, a.s.. This product is indexed under FDA Product Code / Category Classification G020301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 01.01.000.01.03
- Product Code / EMDN
- G020301
- Device Name
- Rektální rourka RIOCATH
- Database Sync Date
- 2026-08-09 16:49:24
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 Rektální rourka RIOCATH modrá?
The registered manufacturer of record for Rektální rourka RIOCATH modrá is Riocath Rectal Tube, a.s..
What is the Primary UDI-DI identifier for Rektální rourka RIOCATH modrá?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593085011419.
What classification code is assigned to this device?
This device is registered under product classification code G020301.
Similar Classification Devices (G020301)
Other Devices by Riocath Rectal Tube, a.s.
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