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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.

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 : B
VLADMIVA Pulpodent
Analysis ID: AKL 20602917454

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Russian Federation

Authorized Representative

PT. TRI ANUGERAH JAYA

AR 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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