Unspecified Brand (UDI 06975474516880)
Manufactured by Pro-med (Beijing) Technology Co., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 1 test/kit) is a medical device manufactured by Pro-med (Beijing) Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0103020401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1 test/kit
- Product Code / EMDN
- W0103020401
- Device Name
- Platelet Mapping AA Kit
- Database Sync Date
- 2026-08-09 16:44:47
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 Pro-med (Beijing) Technology 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 06975474516880.
What classification code is assigned to this device?
This device is registered under product classification code W0103020401.
Similar Classification Devices (W0103020401)
Other Devices by Pro-med (Beijing) Technology Co., Ltd.
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