Dispositivo de Prueba Rápida para Chikungunya IgG/IgM (UDI 06936983126274)
Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.
Device Regulatory Overview
The Dispositivo de Prueba Rápida para Chikungunya IgG/IgM (Model/Catalog Number: ICHI-402) is a medical device manufactured by Hangzhou Alltest Biotech.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
- ICHI-402
- Product Code / EMDN
- W0105099099
- Device Name
- Dispositivo de Prueba Rápida para Chikungunya IgG/IgM
- Database Sync Date
- 2026-08-09 16:45:56
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 Dispositivo de Prueba Rápida para Chikungunya IgG/IgM?
The registered manufacturer of record for Dispositivo de Prueba Rápida para Chikungunya IgG/IgM is Hangzhou Alltest Biotech.Co.,Ltd..
What is the Primary UDI-DI identifier for Dispositivo de Prueba Rápida para Chikungunya IgG/IgM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936983126274.
What classification code is assigned to this device?
This device is registered under product classification code W0105099099.
Similar Classification Devices (W0105099099)
Other Devices by Hangzhou Alltest Biotech.Co.,Ltd.
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