I-Sil Regular Body - Indonesia BPOM Medical Device Registration
I-Sil Regular Body is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420112. 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 MITRA HARAPAN MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SPIDENT CO.,LTDCountry of Origin
Korea
Authorized Representative
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 Light 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
I-Sil Bite
SPIDENT CO.,LTD
I-Sil Putty Premium
SPIDENT CO.,LTD
I-Sil Heavy Body
SPIDENT CO.,LTD
EsCom100 System KIT
SPIDENT CO.,LTD
EsCom250 System KIT
SPIDENT CO.,LTD
Spident FineEtch 37
SPIDENT CO.,LTD
EsTemp NE
SPIDENT CO.,LTD
EsCem
SPIDENT CO.,LTD
Base.it
SPIDENT CO.,LTD
EsTemp
SPIDENT CO.,LTD.

