Pure Global

PREVEST DENPRO HIFLEX Shellac Base Plate - Indonesia BPOM Medical Device Registration

PREVEST DENPRO HIFLEX Shellac Base Plate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602810458. The device is manufactured by PREVEST DENPRO LIMITED. from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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 : A
PREVEST DENPRO HIFLEX Shellac Base Plate
Analysis ID: AKL 10602810458

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

India

Authorized Representative

PT. COBRA DENTAL INDONESIA

AR Address

Jl. Pakuningratan No. 69

Registration Date

Mar 09, 2023

Expiry Date

Jan 10, 2026

Product Type

Prosthetic Dental Equipment

Resin impression tray material.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing