N-terminal pro-B-type Natriuretic Peptide Determination Kit (Fluorescence Immunochromatographic Assay) (UDI 06975182500171)
Manufactured by Beijing Diagreat Biotechnologies Co., Ltd.
Device Regulatory Overview
The N-terminal pro-B-type Natriuretic Peptide Determination Kit (Fluorescence Immunochromatographic Assay) (Model/Catalog Number: P12004) is a medical device manufactured by Beijing Diagreat Biotechnologies Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01021301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P12004
- Product Code / EMDN
- W01021301
- Device Name
- N-terminal pro-B-type Natriuretic Peptide Determination Kit (Fluorescence Immunochromatographic Assay)
- Database Sync Date
- 2026-08-09 16:50:44
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 N-terminal pro-B-type Natriuretic Peptide Determination Kit (Fluorescence Immunochromatographic Assay)?
The registered manufacturer of record for N-terminal pro-B-type Natriuretic Peptide Determination Kit (Fluorescence Immunochromatographic Assay) is Beijing Diagreat Biotechnologies Co., Ltd..
What is the Primary UDI-DI identifier for N-terminal pro-B-type Natriuretic Peptide Determination Kit (Fluorescence Immunochromatographic Assay)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975182500171.
What classification code is assigned to this device?
This device is registered under product classification code W01021301.
Similar Classification Devices (W01021301)
Other Devices by Beijing Diagreat Biotechnologies Co., Ltd.
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