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SLIDE. CHEMILUX Syphilis From - Indonesia BPOM Medical Device Registration

SLIDE. CHEMILUX Syphilis From is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303918685. The device is manufactured by DIA.PRO DIAGNOSTIC BIOPROBES S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SAKEFA.

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.

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Risk Class Kelas Resiko : C
SLIDE. CHEMILUX Syphilis From

DIA.CHEMILUX Syphilis Ab

Analysis ID: AKL 20303918685

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. SAKEFA

AR Address

Jl. Cireunde Raya No.26 Kel. Cireunde Kec. Ciputat Timur

Registration Date

Jan 17, 2020

Expiry Date

Sep 24, 2024

Product Type

Serological Reagents

Treponema pallidum treponemal test reagents.

Invitro Diagnostics

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DJ Fang

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