gudid
Primary ID: KG-1303
M TRACK (UDI KG-1303)
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 M TRACK - Primary ID KG-1303
Device Regulatory Overview
The M TRACK (Model/Catalog Number: KG-1303) is a medical device manufactured by Guangdong KINGFA SCI.&TECH. Co., Ltd.. This product is indexed under FDA Product Code / Category Classification QDO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KG-1303
- Product Code / EMDN
- QDO
- Device Name
- nitrile exam gloves small size
- 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 M TRACK?
The registered manufacturer of record for M TRACK is Guangdong KINGFA SCI.&TECH. Co., Ltd..
What is the Primary UDI-DI identifier for M TRACK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KG-1303.
What classification code is assigned to this device?
This device is registered under product classification code QDO.
Similar Classification Devices (QDO)
Other Devices by Guangdong KINGFA SCI.&TECH. Co., Ltd.
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