Pure Global

VLADMIVA Pulpevit - Indonesia BPOM Medical Device Registration

VLADMIVA Pulpevit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602915580. The device is manufactured by JSC EXPERIMENTAL PLANT VLADMIVA from Russia, and is classified as Risk Class Kelas Resiko : B. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
VLADMIVA Pulpevit
Analysis ID: AKL 20602915580

Risk Classification

Kelas Resiko : B

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

Sep 07, 2023

Expiry Date

Jun 15, 2028

Product Type

Prosthetic Dental Equipment

Coating material for resin fillings.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name