VLADMIVA Pulpodent - Indonesia BPOM Medical Device Registration
VLADMIVA Pulpodent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602917454. The device is manufactured by JSC EXPERIMENTAL PLANT VLADMIVA from Russian Federation, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRI ANUGERAH JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JSC EXPERIMENTAL PLANT VLADMIVACountry of Origin
Russian Federation
Authorized Representative
PT. TRI ANUGERAH JAYAAR Address
Jl. Raya Pos Pengumben 34 G, RT/RW 002/005
Registration Date
Aug 28, 2023
Expiry Date
Jun 15, 2028
Product Type
Prosthetic Dental Equipment
Dental cement.
Non Electromedic Non Sterile
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