Pure Global

MEDENTAL Flowable Composite - Indonesia BPOM Medical Device Registration

MEDENTAL Flowable Composite is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602818490. The device is manufactured by CONAMCO SA DE CV DBA MEDENTAL. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL DENT.

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 : B
MEDENTAL Flowable Composite
Analysis ID: AKL 20602818490

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. GLOBAL DENT

AR Address

JALAN KYAI MAJA NO 65 RT 001 / RW 002 KRAMAT PELA, KEBAYORAN BARU JAKARTA SELATAN

Registration Date

Dec 15, 2023

Expiry Date

Dec 31, 2028

Product Type

Prosthetic Dental Equipment

Tooth shade resin material.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from CONAMCO SA DE CV DBA MEDENTAL.
Products from the same manufacturer (2 products)