Vietnam MOH registration 240002166/PCBB-HN

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
Vietnam flagVietnam·Risk Class TTBYT Loại B·Theo theo phụ lục·BALIO Diagnostics·Registered Aug 26, 2024
Registration details
Analysis ID
240002166/PCBB-HN
Submission ID
000.00.19.H26-240612-0021
Product Type
Theo theo phụ lục
Product Code
Theo phụ lục
Company information
Manufacturer
BALIO Diagnostics
Manufacturer Country
Theo theo phụ lục
Product Owner
BALIO Diagnostics
Authorized Representative
CÔNG TY CỔ PHẦN VSENS
Technical details
Intended Use
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
Registration Date
Aug 26, 2024
About this record

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.

Free DatabasePowered by Pure Global AI300,000+ Devices