eudamed_udi
Primary ID: 06935740733434
Unspecified Brand (UDI 06935740733434)
Manufactured by URIT Medical Electronic Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06935740733434
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: /) is a medical device manufactured by URIT Medical Electronic Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W01010221 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- W01010221
- Device Name
- Low-density Lipoprotein Cholesterol Reagent Kit (Direct Method-Surfactant Removal Method)
- Database Sync Date
- 2026-08-09 16:49:53
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 URIT Medical Electronic 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 06935740733434.
What classification code is assigned to this device?
This device is registered under product classification code W01010221.
Similar Classification Devices (W01010221)
Other Devices by URIT Medical Electronic Co.,Ltd.
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