Spident FineEtch 37 - Indonesia BPOM Medical Device Registration
Spident FineEtch 37 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220365. 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 2nd Floor Unit 69-71 Jl. Letjen Soepeno No 34 Arteri Permata Hijau, Jakarta 12210 Indonesia
Registration Date
Nov 23, 2022
Expiry Date
Dec 31, 2026
Product Type
Prosthetic Dental Equipment
Tooth shade resin material.
Non Electromedic Non Sterile
I-Sil Bite
I-Sil Regular Body
I-SIL Light Body
I-Sil Putty Premium
I-Sil Heavy Body
EsCom100 System KIT
EsCom250 System KIT
SPIDENT NOP
Temp.it Light Curing Temporary Filling Material
SPIDENT FineDam
I-Sil Bite
SPIDENT CO.,LTD
I-Sil Putty Premium
SPIDENT CO.,LTD
I-Sil Regular Body
SPIDENT CO.,LTD
I-Sil Heavy Body
SPIDENT CO.,LTD
EsCom100 System KIT
SPIDENT CO.,LTD
EsCom250 System KIT
SPIDENT CO.,LTD
EsTemp NE
SPIDENT CO.,LTD
EsCem
SPIDENT CO.,LTD
Base.it
SPIDENT CO.,LTD
EsTemp
SPIDENT CO.,LTD.

