Myoglobin (Myo) Test Kit (Immunofluorescence) (UDI 06978198482233)
Manufactured by Shenzhen Huiyan Sci-Tech Biotechnology Co., Ltd.
Device Regulatory Overview
The Myoglobin (Myo) Test Kit (Immunofluorescence) (Model/Catalog Number: 2223) is a medical device manufactured by Shenzhen Huiyan Sci-Tech Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01021304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2223
- Product Code / EMDN
- W01021304
- Device Name
- Myoglobin (Myo) Test Kit (Immunofluorescence)
- Database Sync Date
- 2026-08-09 16:47:19
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 Myoglobin (Myo) Test Kit (Immunofluorescence)?
The registered manufacturer of record for Myoglobin (Myo) Test Kit (Immunofluorescence) is Shenzhen Huiyan Sci-Tech Biotechnology Co., Ltd..
What is the Primary UDI-DI identifier for Myoglobin (Myo) Test Kit (Immunofluorescence)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978198482233.
What classification code is assigned to this device?
This device is registered under product classification code W01021304.
Similar Classification Devices (W01021304)
Other Devices by Shenzhen Huiyan Sci-Tech Biotechnology Co., Ltd.
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