gudid
Primary ID: RFK-C101020BU
cannulaEchoRF (UDI RFK-C101020BU)
Manufactured by COSMAN MEDICAL, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for cannulaEchoRF - Primary ID RFK-C101020BU
Device Regulatory Overview
The cannulaEchoRF (Model/Catalog Number: RFK-C101020BU) is a medical device manufactured by COSMAN MEDICAL, LLC. This product is indexed under FDA Product Code / Category Classification GXI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RFK-C101020BU
- Product Code / EMDN
- GXI
- Device Name
- Cannula 10cm, 10mm Tip, 20G
- Database Sync Date
- 2026-08-09 09:10:55
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 cannulaEchoRF?
The registered manufacturer of record for cannulaEchoRF is COSMAN MEDICAL, LLC.
What is the Primary UDI-DI identifier for cannulaEchoRF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RFK-C101020BU.
What classification code is assigned to this device?
This device is registered under product classification code GXI.
Similar Classification Devices (GXI)
Other Devices by COSMAN MEDICAL, LLC
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