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ALLPLEX™ HPV28 Detection - Indonesia BPOM Medical Device Registration

ALLPLEX™ HPV28 Detection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306320359. The device is manufactured by SEEGENE INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SCIENCEWERKE.

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BPOM Registered
Risk Class Kelas Resiko : C
ALLPLEX™ HPV28 Detection
Analysis ID: AKL 20306320359

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SEEGENE INC.

Country of Origin

Korea

Authorized Representative

PT. SCIENCEWERKE

AR Address

Jl.Palmerah Barat No.25

Registration Date

Dec 05, 2023

Expiry Date

Aug 30, 2025

Product Type

Tumor Antigen Immunologic Test System

Dna Detection for Human Papillomavirus

Invitro Diagnostics

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