CRP Control (UDI 06974521000402)
Manufactured by Shenzhen Superbio Technology Co.,Ltd.
Device Regulatory Overview
The CRP Control (Model/Catalog Number: QC402) is a medical device manufactured by Shenzhen Superbio Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102152003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- QC402
- Product Code / EMDN
- W0102152003
- Device Name
- CRP Control
- Database Sync Date
- 2026-08-09 16:49:16
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 CRP Control?
The registered manufacturer of record for CRP Control is Shenzhen Superbio Technology Co.,Ltd..
What is the Primary UDI-DI identifier for CRP Control?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974521000402.
What classification code is assigned to this device?
This device is registered under product classification code W0102152003.
Similar Classification Devices (W0102152003)
Other Devices by Shenzhen Superbio Technology Co.,Ltd.
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