NEOCOLLOID - Indonesia BPOM Medical Device Registration
NEOCOLLOID is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420186. The device is manufactured by ZHERMACK S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DENTSPLY SIRONA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHERMACK S.P.A.Country of Origin
Italy
Authorized Representative
DENTSPLY SIRONA INDONESIAAR Address
Gedung Tempo Scan Tower, Lantai 28, Jl. H.R. Rasuna Said Kav. 3-4
Registration Date
Apr 25, 2024
Expiry Date
Feb 05, 2029
Product Type
Prosthetic Dental Equipment
Impression material.
Non Electromedic Non Sterile
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