eudamed_udi
Primary ID: 06945095540830
SLT (UDI 06945095540830)
Manufactured by Zumax Medical CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SLT - Primary ID 06945095540830
Device Regulatory Overview
The SLT (Model/Catalog Number: 50DB3555) is a medical device manufactured by Zumax Medical CO., LTD.. This product is indexed under FDA Product Code / Category Classification Q0299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 50DB3555
- Product Code / EMDN
- Q0299
- Device Name
- Binocular Loupes
- Database Sync Date
- 2026-08-09 16:29:15
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 SLT?
The registered manufacturer of record for SLT is Zumax Medical CO., LTD..
What is the Primary UDI-DI identifier for SLT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945095540830.
What classification code is assigned to this device?
This device is registered under product classification code Q0299.
Similar Classification Devices (Q0299)
Other Devices by Zumax Medical CO., LTD.
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