gudid
Primary ID: CC15521U
cannulaEchoRF (UDI CC15521U)
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 CC15521U
Device Regulatory Overview
The cannulaEchoRF (Model/Catalog Number: CC15521U) 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
- CC15521U
- Product Code / EMDN
- GXI
- Device Name
- Cannula 15cm, 5mm Tip, 21G
- Database Sync Date
- 2026-08-09 09:10:55
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 CC15521U.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint