ImproClot®Thrombelastograph (UDI 06974481833393)
Manufactured by Guangzhou Improve Medical Instruments Co., Ltd
Device Regulatory Overview
The ImproClot®Thrombelastograph (Model/Catalog Number: 310202000) is a medical device manufactured by Guangzhou Improve Medical Instruments Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0202020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 310202000
- Product Code / EMDN
- W0202020101
- Device Name
- Thrombelastograph
- Database Sync Date
- 2026-08-09 16:58:36
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 ImproClot®Thrombelastograph?
The registered manufacturer of record for ImproClot®Thrombelastograph is Guangzhou Improve Medical Instruments Co., Ltd.
What is the Primary UDI-DI identifier for ImproClot®Thrombelastograph?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974481833393.
What classification code is assigned to this device?
This device is registered under product classification code W0202020101.
Similar Classification Devices (W0202020101)
Other Devices by Guangzhou Improve Medical Instruments Co., Ltd
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