gudid
Primary ID: MD5940
G.LAB (UDI MD5940)
Manufactured by Grandway Technology (Shenzhen) Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for G.LAB - Primary ID MD5940
Device Regulatory Overview
The G.LAB (Model/Catalog Number: MD5940) is a medical device manufactured by Grandway Technology (Shenzhen) Limited. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MD5940
- Product Code / EMDN
- DXN
- Device Name
- Database Sync Date
- 2026-08-09 09:46:04
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 G.LAB?
The registered manufacturer of record for G.LAB is Grandway Technology (Shenzhen) Limited.
What is the Primary UDI-DI identifier for G.LAB?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MD5940.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Other Devices by Grandway Technology (Shenzhen) Limited
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