IMPROVACUTER® Evacuated Blood Collection Tube (UDI 06974481833461)
Manufactured by Guangzhou Improve Medical Instruments Co., Ltd
Device Regulatory Overview
The IMPROVACUTER® Evacuated Blood Collection Tube (Model/Catalog Number: 613060202;613060242;613060202A;613060202D) is a medical device manufactured by Guangzhou Improve Medical Instruments Co., Ltd. This product is indexed under FDA Product Code / Category Classification W050101010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 613060202;613060242;613060202A;613060202D
- Product Code / EMDN
- W050101010201
- Device Name
- Evacuated Blood Collection Tube
- Database Sync Date
- 2026-08-09 16:48:17
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 IMPROVACUTER® Evacuated Blood Collection Tube?
The registered manufacturer of record for IMPROVACUTER® Evacuated Blood Collection Tube is Guangzhou Improve Medical Instruments Co., Ltd.
What is the Primary UDI-DI identifier for IMPROVACUTER® Evacuated Blood Collection Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974481833461.
What classification code is assigned to this device?
This device is registered under product classification code W050101010201.
Similar Classification Devices (W050101010201)
Other Devices by Guangzhou Improve Medical Instruments Co., Ltd
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