SYNTEX - Indonesia BPOM Medical Device Registration
SYNTEX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220014. The device is manufactured by PPH CERKAMED WOJCIECH PAWLOWSKI from Poland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. THOMASONG NIRMALA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PPH CERKAMED WOJCIECH PAWLOWSKICountry of Origin
Poland
Authorized Representative
PT. THOMASONG NIRMALAAR Address
Jl. AM. Sangaji No. 20A
Registration Date
Feb 19, 2024
Expiry Date
Oct 13, 2027
Product Type
Prosthetic Dental Equipment
Root canal filling resin
Non Electromedic Non Sterile
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