Fecal Occult Blood (FOB) Quantitative Detection Kit (Immunochromatographic Assay) (UDI 06971348763237)
Manufactured by Shenzhen Microprofit Biotech Co., Ltd
Device Regulatory Overview
The Fecal Occult Blood (FOB) Quantitative Detection Kit (Immunochromatographic Assay) (Model/Catalog Number: MF-126-20) is a medical device manufactured by Shenzhen Microprofit Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102039013 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MF-126-20
- Product Code / EMDN
- W0102039013
- Device Name
- Fecal Occult Blood (FOB) Quantitative Detection Kit (Immunochromatographic Assay)
- Database Sync Date
- 2026-08-09 16:29:45
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 Fecal Occult Blood (FOB) Quantitative Detection Kit (Immunochromatographic Assay)?
The registered manufacturer of record for Fecal Occult Blood (FOB) Quantitative Detection Kit (Immunochromatographic Assay) is Shenzhen Microprofit Biotech Co., Ltd.
What is the Primary UDI-DI identifier for Fecal Occult Blood (FOB) Quantitative Detection Kit (Immunochromatographic Assay)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971348763237.
What classification code is assigned to this device?
This device is registered under product classification code W0102039013.
Similar Classification Devices (W0102039013)
Other Devices by Shenzhen Microprofit Biotech Co., Ltd
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