Vietnam MOH registration 220004142/PCBB-HCM

IVD Department Qualitative IgG Antibody Test for Dog Roundworm Toxocara canis

VN: Bộ IVD xét nghiệm định tính kháng thể IgG kháng giun đũa chó Toxocara canis

Vitrotest® Anti- Toxocara

Vietnam·Risk Class TTBYT Loại B·Vitrotest Anti- Toxocara·Vitrotest Bioreagent LLC·Registered Dec 30, 2022

Registration details

Analysis ID: 220004142/PCBB-HCM
Submission ID: 000.00.19.H29-221227-0011
Product Type: Vitrotest Anti- Toxocara
Product Code: TK058

Company information

Manufacturer: Vitrotest Bioreagent LLC

Technical details

Intended Use: The IVD qualitative IgG antibody test for Toxocara canis is a Enzyme-Linked Immunosorbent Assay (ELISA) to detect the presence of IgG antibodies against Toxocara canis in human serum or plasma.

Dates and status

Registration Date: Dec 30, 2022

About this record

Access comprehensive regulatory information for IVD Department Qualitative IgG Antibody Test for Dog Roundworm Toxocara canis 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 220004142/PCBB-HCM and manufactured by Vitrotest Bioreagent LLC.

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.