Pure Global

UNI-MEDICA Nucleic Acid Extraction Reagent Manual - Indonesia BPOM Medical Device Registration

UNI-MEDICA Nucleic Acid Extraction Reagent Manual is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204125055. The device is manufactured by SHENZHEN UNI-MEDICA TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. RAJAERBA INDOCHEM.

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 : A
UNI-MEDICA Nucleic Acid Extraction Reagent Manual
Analysis ID: AKL 10204125055

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. RAJAERBA INDOCHEM

AR Address

GEDUNG PEMBINA GRAHA JL. DI. PANJAITAN NO.45 RAWA BUNGA

Registration Date

Aug 18, 2021

Expiry Date

Feb 01, 2024

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing