eudamed_udi
Primary ID: 06975424223653
Unspecified Brand (UDI 06975424223653)
Manufactured by DiYaLab ZJG Biotech Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06975424223653
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: DL190805) is a medical device manufactured by DiYaLab ZJG Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W01021301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DL190805
- Product Code / EMDN
- W01021301
- Device Name
- N-terminal pro-brain nitric peptide Assay Kit (Fluorescence Immunoassay)
- Database Sync Date
- 2026-08-09 16:49:40
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is DiYaLab ZJG Biotech Co., Ltd.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975424223653.
What classification code is assigned to this device?
This device is registered under product classification code W01021301.
Similar Classification Devices (W01021301)
Other Devices by DiYaLab ZJG Biotech Co., Ltd
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