gudid
Primary ID: M6576-02/10
Cortex Removal Cannulae (UDI M6576-02/10)
Manufactured by STERIMEDIX LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cortex Removal Cannulae - Primary ID M6576-02/10
Device Regulatory Overview
The Cortex Removal Cannulae (Model/Catalog Number: M6576-02/10) is a medical device manufactured by STERIMEDIX LIMITED. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M6576-02/10
- Product Code / EMDN
- MED
- Device Name
- 23g x 7/8" Cortex Ext
- Database Sync Date
- 2026-08-09 09:16:45
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 Cortex Removal Cannulae?
The registered manufacturer of record for Cortex Removal Cannulae is STERIMEDIX LIMITED.
What is the Primary UDI-DI identifier for Cortex Removal Cannulae?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M6576-02/10.
What classification code is assigned to this device?
This device is registered under product classification code MED.
Similar Classification Devices (MED)
Other Devices by STERIMEDIX LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint