gudid
Primary ID: L4952
zumax (UDI L4952)
Manufactured by Zumax Medical Co., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for zumax - Primary ID L4952
Device Regulatory Overview
The zumax (Model/Catalog Number: L4952) is a medical device manufactured by Zumax Medical Co., LTD. This product is indexed under FDA Product Code / Category Classification HLJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L4952
- Product Code / EMDN
- HLJ
- Device Name
- 2.5V LED bulb
- Database Sync Date
- 2026-08-09 09:11:04
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 zumax?
The registered manufacturer of record for zumax is Zumax Medical Co., LTD.
What is the Primary UDI-DI identifier for zumax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L4952.
What classification code is assigned to this device?
This device is registered under product classification code HLJ.
Similar Classification Devices (HLJ)
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