gudid
Primary ID: M5584-02/5
Coaxial Cannulae and Hand Pieces (UDI M5584-02/5)
Manufactured by STERIMEDIX LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Coaxial Cannulae and Hand Pieces - Primary ID M5584-02/5
Device Regulatory Overview
The Coaxial Cannulae and Hand Pieces (Model/Catalog Number: M5584-02/5) 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
- M5584-02/5
- Product Code / EMDN
- MED
- Device Name
- 16/21g I/A Handpiece 90
- Database Sync Date
- 2026-08-09 09:59:20
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 Coaxial Cannulae and Hand Pieces?
The registered manufacturer of record for Coaxial Cannulae and Hand Pieces is STERIMEDIX LIMITED.
What is the Primary UDI-DI identifier for Coaxial Cannulae and Hand Pieces?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M5584-02/5.
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
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