gudid
Primary ID: M2280-02/10
Anterior Chamber Maintenance Cannulae (UDI M2280-02/10)
Manufactured by STERIMEDIX LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anterior Chamber Maintenance Cannulae - Primary ID M2280-02/10
Device Regulatory Overview
The Anterior Chamber Maintenance Cannulae (Model/Catalog Number: M2280-02/10) 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
- M2280-02/10
- Product Code / EMDN
- MED
- Device Name
- 27g x 7/8" Transzonular
- Database Sync Date
- 2026-08-09 09:22:52
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 Anterior Chamber Maintenance Cannulae?
The registered manufacturer of record for Anterior Chamber Maintenance Cannulae is STERIMEDIX LIMITED.
What is the Primary UDI-DI identifier for Anterior Chamber Maintenance Cannulae?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M2280-02/10.
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
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