SANITY 2.0 System - Indonesia BPOM Medical Device Registration

SANITY 2.0 System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304220083. The device is manufactured by XIAMEN ZEESAN BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRINISYAH ERSA PRATAMA.

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BPOM Registered

Risk Class Kelas Resiko : C

SANITY 2.0 System

Analysis ID: AKL 20304220083

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

XIAMEN ZEESAN BIOTECH CO., LTD.

Country of Origin

China

Authorized Representative

PT. TRINISYAH ERSA PRATAMA

AR Address

Menara Karya Lantai 16 Jl. HR Rasuna Said Blok X.5 Kaveling 1-2

Registration Date

Aug 29, 2022

Expiry Date

Nov 18, 2023

Product Type

Immunology Laboratory Equipment and Reagents

RNA Preanalytical Systems.

Invitro Diagnostics

DJ Fang

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