Pure Global

DENFIL Light-Cured Hybrid Composite Resin - Indonesia BPOM Medical Device Registration

DENFIL Light-Cured Hybrid Composite Resin is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602915614. The device is manufactured by VERICOM CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PROSPEROUS DENTAL CAB.

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
DENFIL Light-Cured Hybrid Composite Resin
Analysis ID: AKL 20602915614

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VERICOM CO., LTD

Country of Origin

Korea

Authorized Representative

PROSPEROUS DENTAL CAB

AR Address

Taman Kopo Indah II Blok E.2 nomor 4 & 5, RT. 010/RW. 017

Registration Date

Oct 18, 2023

Expiry Date

Jul 24, 2028

Product Type

Prosthetic Dental Equipment

Dental cement.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from VERICOM CO., LTD
Products from the same manufacturer (2 products)