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IVD Department Quantitative Fibrinogen Testing - Vietnam Registration 230000173/PCBB-BYT

Access comprehensive regulatory information for IVD Department Quantitative Fibrinogen Testing in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 230000173/PCBB-BYT and manufactured by Theo theo phụ lục.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Siemens Healthineers, and 1 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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230000173/PCBB-BYT
Registration Details
Vietnam MOH Registration: 230000173/PCBB-BYT
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Device Details

IVD Department Quantitative Fibrinogen Testing
VN: Bộ IVD xét nghiệm định lượng Fibrinogen
Risk Class TTBYT Loại B

Registration Details

230000173/PCBB-BYT

000.00.04.G18-220815-0008

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

Technical Details

1. Fibrinogen: A test used to determine the amount of fibrinogen in human serum. 2. Fibrinogen Calibrator: Used in the construction of the reference calibration curve in the quantitative determination of fibrinogen in citrated serum by turbidimetric and nephelometric immunoassay. The calibrator is used in combination with the Centronic Fibrinogen kit. 3. Fibrinogen Control: Control material for accuracy in the quantitative determination of fibrinogen in citrated serum by turbidimetry and nephelometry.

Dates and Status

Feb 28, 2023

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