Pure Global

VIRTUE DX Syphilis TP Reagent Kit - Indonesia BPOM Medical Device Registration

VIRTUE DX Syphilis TP Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321274. The device is manufactured by VIRTUE DIAGNOSTICS SUZHOU CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DARMA LABORA INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
VIRTUE DX Syphilis TP Reagent Kit
Analysis ID: AKL 20303321274

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DARMA LABORA INDONESIA

AR Address

KAWASAN INDUSTRI JABABEKA 7, BLOK B3/B, DESA WANGUNHARJA

Registration Date

Jan 14, 2025

Expiry Date

Mar 02, 2028

Product Type

Serological Reagents

Treponema pallidum treponemal test reagents.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing