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IVD Department Qualitative IgG Antibody Test for Dog Roundworm Toxocara canis - Vietnam Registration 220004142/PCBB-HCM

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 Loแบกi 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.

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220004142/PCBB-HCM
Registration Details
Vietnam MOH Registration: 220004142/PCBB-HCM
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Device Details

IVD Department Qualitative IgG Antibody Test for Dog Roundworm Toxocara canis
VN: Bแป™ IVD xรฉt nghiแป‡m ฤ‘แป‹nh tรญnh khรกng thแปƒ IgG khรกng giun ฤ‘ลฉa chรณ Toxocara canis
Vitrotestยฎ Anti- Toxocara
Risk Class TTBYT Loแบกi B

Registration Details

220004142/PCBB-HCM

000.00.19.H29-221227-0011

Vitrotest Anti- Toxocara

TK058

Company Information

Technical Details

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

Dec 30, 2022