Pure Global

MAXGENOL - Indonesia BPOM Medical Device Registration

MAXGENOL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602122060. The device is manufactured by PREVEST DENPRO LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is COBRA DENTAL INDONESIA.

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 : C
MAXGENOL
Analysis ID: AKL 20602122060

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

PREVEST DENPRO LTD

Country of Origin

India

Authorized Representative

COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

Feb 16, 2023

Expiry Date

Jan 16, 2026

Product Type

Prosthetic Dental Equipment

Root canal filling resin

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing