3M ESPE Imprint 4 Regular - Indonesia BPOM Medical Device Registration
3M ESPE Imprint 4 Regular is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602910155. The device is manufactured by 3M DEUTSCHLAND GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 3M INDONESIA IMPORTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
3M DEUTSCHLAND GMBH.Country of Origin
Germany
Authorized Representative
PT. 3M INDONESIA IMPORTAMAAR Address
Perkantoran Hijau Arkadia Tower F Lt.8-B, Jl.Letjen TB Simatupang Kav.88
Registration Date
Oct 20, 2023
Expiry Date
Feb 16, 2027
Product Type
Prosthetic Dental Equipment
Impression material.
Non Electromedic Non Sterile
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