Pure Global

HUMAROCK - Indonesia BPOM Medical Device Registration

HUMAROCK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102220228. The device is manufactured by DLAB SCIENTIFIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SALI POLAPA TOGETHER.

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
HUMAROCK
Analysis ID: AKL 10102220228

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SALI POLAPA TOGETHER

AR Address

Puri Sentra Niaga Blok B 33-34 Jl. Raya Kalimalang 13620

Registration Date

Sep 12, 2022

Expiry Date

Dec 31, 2024

Product Type

Clinical Laboratory Equipment

General purpose laboratory equipment labeled or promoted for a specific medical use. (Electrically operated)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing