Pure Global

STANDARD™ Q Rotavirus Ag Test - Indonesia BPOM Medical Device Registration

STANDARD™ Q Rotavirus Ag Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303911248. The device is manufactured by SD BIOSENSOR from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is STANDARD BIOSENSOR 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 : B
STANDARD™ Q Rotavirus Ag Test
Analysis ID: AKL 20303911248

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SD BIOSENSOR

Country of Origin

Korea

Authorized Representative

STANDARD BIOSENSOR INDONESIA

AR Address

L'Avenue Office Tower Lt.21 Unit C, Jl. Raya Pasar Minggu Kav.16 Kel. Pancoran Kec. Pancoran , Jakarta Selatan

Registration Date

May 31, 2022

Expiry Date

Dec 30, 2025

Product Type

Serological Reagents

Poliovirus serological reagents.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing