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KAZAMA ENT Unit - Indonesia BPOM Medical Device Registration

KAZAMA ENT Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10704220017. The device is manufactured by KAZAMAENT CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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 : A
KAZAMA ENT Unit
Analysis ID: AKL 10704220017

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

May 12, 2022

Expiry Date

May 01, 2026

Product Type

Therapeutic Ear, Nose and Throat Equipment

Ear, nose, and throat examination and treatment unit.

Non Radiation Electromedics

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