gudid
Primary ID: M4503-02/5
Vitreoretinal Handpieces (UDI M4503-02/5)
Manufactured by STERIMEDIX LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vitreoretinal Handpieces - Primary ID M4503-02/5
Device Regulatory Overview
The Vitreoretinal Handpieces (Model/Catalog Number: M4503-02/5) 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
- M4503-02/5
- Product Code / EMDN
- MED
- Device Name
- Backflush/25g Soft Tip
- 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 Vitreoretinal Handpieces?
The registered manufacturer of record for Vitreoretinal Handpieces is STERIMEDIX LIMITED.
What is the Primary UDI-DI identifier for Vitreoretinal Handpieces?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M4503-02/5.
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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