IMPROSAFE® ImPress Blood Collection Set (UDI 06978565410524)
Manufactured by Guangzhou Improve Medical Instruments Co., Ltd
Device Regulatory Overview
The IMPROSAFE® ImPress Blood Collection Set (Model/Catalog Number: 5991213002) is a medical device manufactured by Guangzhou Improve Medical Instruments Co., Ltd. This product is indexed under FDA Product Code / Category Classification A010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5991213002
- Product Code / EMDN
- A010199
- Device Name
- Blood Collection Needle
- Database Sync Date
- 2026-08-09 16:30:07
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 IMPROSAFE® ImPress Blood Collection Set?
The registered manufacturer of record for IMPROSAFE® ImPress Blood Collection Set is Guangzhou Improve Medical Instruments Co., Ltd.
What is the Primary UDI-DI identifier for IMPROSAFE® ImPress Blood Collection Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978565410524.
What classification code is assigned to this device?
This device is registered under product classification code A010199.
Similar Classification Devices (A010199)
Other Devices by Guangzhou Improve Medical Instruments Co., Ltd
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