gudid
Primary ID: DM6BE
zumax (UDI DM6BE)
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 DM6BE
Device Regulatory Overview
The zumax (Model/Catalog Number: DM6BE) 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
- DM6BE
- Product Code / EMDN
- HLJ
- Device Name
- Database Sync Date
- 2026-08-09 09:11:03
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 DM6BE.
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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