Pure Global

VAZYME Automatic Flourescence Immunoassay Analyzer - Indonesia BPOM Medical Device Registration

VAZYME Automatic Flourescence Immunoassay Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304220048. The device is manufactured by NANJING VAZYME MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HEALTHY FAMILY FOCUS.

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 : B
VAZYME Automatic Flourescence Immunoassay Analyzer
Analysis ID: AKL 20304220048

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HEALTHY FAMILY FOCUS

AR Address

Komplek Delta Building Blok B 1-2, Jalan Suryopranoto No. 1-9

Registration Date

May 25, 2022

Expiry Date

Mar 08, 2027

Product Type

Immunology Laboratory Equipment and Reagents

Immunofluorometer equipment

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing