Chikungunya IgG/IgM Rapid Test(Whole Blood/Serum/Plasma) (UDI D-697424646CHIK000N38V)
Manufactured by SAFECARE BIOTECH (HANGZHOU) CO., LTD.
Device Regulatory Overview
The Chikungunya IgG/IgM Rapid Test(Whole Blood/Serum/Plasma) (Model/Catalog Number: CHIK-4022) is a medical device manufactured by SAFECARE BIOTECH (HANGZHOU) CO., LTD.. This product is indexed under FDA Product Code / Category Classification W0105099099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CHIK-4022
- Product Code / EMDN
- W0105099099
- Device Name
- Chikungunya IgG/IgM Rapid Test(Whole Blood/Serum/Plasma)
- Database Sync Date
- 2026-08-09 16:29:09
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 Chikungunya IgG/IgM Rapid Test(Whole Blood/Serum/Plasma)?
The registered manufacturer of record for Chikungunya IgG/IgM Rapid Test(Whole Blood/Serum/Plasma) is SAFECARE BIOTECH (HANGZHOU) CO., LTD..
What is the Primary UDI-DI identifier for Chikungunya IgG/IgM Rapid Test(Whole Blood/Serum/Plasma)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-697424646CHIK000N38V.
What classification code is assigned to this device?
This device is registered under product classification code W0105099099.
Similar Classification Devices (W0105099099)
Other Devices by SAFECARE BIOTECH (HANGZHOU) CO., LTD.
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