gudid
Primary ID: KG-1801(GNM-XM)
AURA (UDI KG-1801(GNM-XM))
Manufactured by Guangdong KINGFA SCI.&TECH. Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AURA - Primary ID KG-1801(GNM-XM)
Device Regulatory Overview
The AURA (Model/Catalog Number: KG-1801(GNM-XM)) is a medical device manufactured by Guangdong KINGFA SCI.&TECH. Co., Ltd.. This product is indexed under FDA Product Code / Category Classification LZA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KG-1801(GNM-XM)
- Product Code / EMDN
- LZA
- Device Name
- Aura Exam Premium Nitrile Examination Gloves:KG-1801(GNS-XM\GNM-XM\GNL-XM\GNXL-XM)
- Database Sync Date
- 2026-08-09 09:21:56
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 AURA?
The registered manufacturer of record for AURA is Guangdong KINGFA SCI.&TECH. Co., Ltd..
What is the Primary UDI-DI identifier for AURA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KG-1801(GNM-XM).
What classification code is assigned to this device?
This device is registered under product classification code LZA.
Similar Classification Devices (LZA)
Other Devices by Guangdong KINGFA SCI.&TECH. Co., Ltd.
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