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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.

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BPOM Registered
Risk Class Kelas Resiko : C
PULPEVIT
Analysis ID: AKL 20602913962

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Russia

Authorized Representative

TRI ANUGERAH JAYA

AR 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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