I-SIL Light Body - Indonesia BPOM Medical Device Registration
I-SIL Light Body is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420111. The device is manufactured by SPIDENT CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MITRA HARAPAN MANDIRI.
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
SPIDENT CO.,LTDCountry of Origin
Korea
Authorized Representative
PT. MITRA HARAPAN MANDIRIAR Address
The Bellezza Shopping Arcade Lt. 2 SA 69, 70 & 71, Jl. Letjen Soepeno No. 34 Arteri Permata Hijau
Registration Date
Feb 21, 2024
Expiry Date
Dec 31, 2026
Product Type
Prosthetic Dental Equipment
Impression material.
Non Electromedic Non Sterile
I-Sil Bite
I-Sil Putty Premium
I-Sil Regular Body
I-Sil Heavy Body
EsCom250 System KIT
EsCom100 System KIT
SPIDENT NOP
Temp.it Light Curing Temporary Filling Material
SPIDENT FineDam
Spident FineEtch 37
WOWART COG
DERMALINE CO., LTD.
WOWART MONO
DERMALINE CO., LTD.
ESFLOW Light Curing Flowable Composite Resin
SPIDENT CO.,LTD.
ESCOM100 Light-Cured Restorative Nano-Hybrid Composite Resin
SPIDENT CO.,LTD.
ORA-AID Intra-Oral Wound Dressing
TBM CORPORATION
HEXA-TEMP Temporary Crown and Bridge Resin
SPIDENT CO.,LTD.
SPIDENT EsCom250
SPIDENT CO.,LTD.
MIHO Fill M900
SCL CO.,LTD
MIHO Fill M600
SCL CO.,LTD
MIHO Fill M400
SCL CO., LTD

