Unspecified Brand (UDI D-K91201-054A)
Manufactured by SHENZHEN REETOO BIOTECHNOLOGY CO., LTD
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: /) is a medical device manufactured by SHENZHEN REETOO BIOTECHNOLOGY CO., LTD. This product is indexed under FDA Product Code / Category Classification W01021109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- W01021109
- Device Name
- Full Range C-reactive Protein (FR-CRP) Assay Kit (Nephelometry)
- Database Sync Date
- 2026-08-09 16:28:50
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 SHENZHEN REETOO BIOTECHNOLOGY 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 D-K91201-054A.
What classification code is assigned to this device?
This device is registered under product classification code W01021109.
Similar Classification Devices (W01021109)
Other Devices by SHENZHEN REETOO BIOTECHNOLOGY CO., LTD
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