PULPEVIT - Indonesia BPOM Medical Device Registration
PULPEVIT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602913962. The device is manufactured by JSC EXPERIMENTAL PLANT VLADMIVA from Russia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRI ANUGERAH JAYA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
JSC EXPERIMENTAL PLANT VLADMIVACountry of Origin
Russia
Authorized Representative
TRI ANUGERAH JAYAAR Address
Jl. Raya Pos Pengumben 34 G, RT/RW 002/005
Registration Date
Aug 17, 2023
Expiry Date
Jun 15, 2028
Product Type
Prosthetic Dental Equipment
Root canal filling resin
Non Electromedic Non Sterile
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