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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
VERICOM CO., LTDCountry of Origin
Korea
Authorized Representative
PROSPEROUS DENTAL CABAR 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
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