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Drug Testing, Control Material, Diagnostic Reference Standard for In Vitro Use in Hematology Analyzers - Vietnam Registration 240002166/PCBB-HN

Access comprehensive regulatory information for Drug Testing, Control Material, Diagnostic Reference Standard for In Vitro Use in Hematology Analyzers 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 240002166/PCBB-HN and manufactured by BALIO Diagnostics. The authorized representative in Vietnam is CÔNG TY CỔ PHẦN VSENS.

This page provides complete technical specifications, regulatory compliance details. 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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240002166/PCBB-HN
Registration Details
Vietnam MOH Registration: 240002166/PCBB-HN
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Device Details

Drug Testing, Control Material, Diagnostic Reference Standard for In Vitro Use in Hematology Analyzers
VN: Thuốc thử, vật liệu kiểm soát, chất hiệu chuẩn chẩn đoán Invitro sử dụng cho máy phân tích huyết học
Thuốc thử, vật liệu kiểm soát, chất hiệu chuẩn chẩn đoán Invitro sử dụng cho máy phân tích huyết học
Risk Class TTBYT Loại B

Registration Details

240002166/PCBB-HN

000.00.19.H26-240612-0021

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

BALIO Diagnostics

Technical Details

Chemicals run the diagnostic tests Invitro, combined with the biochemical analysis machine, to produce data that are then used to evaluate and diagnose the patient's condition, in order to determine the appropriate treatment.

Dates and Status

Aug 26, 2024