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KIVERSAL Audiometric Booths K-Series - Indonesia BPOM Medical Device Registration

KIVERSAL Audiometric Booths K-Series is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10701320058. The device is manufactured by DEVIMETRIX S.L. from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MAIN MEDICAL PARTNERS.

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
KIVERSAL Audiometric Booths K-Series
Analysis ID: AKL 10701320058

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DEVIMETRIX S.L.

Country of Origin

Spain

Authorized Representative

PT. MAIN MEDICAL PARTNERS

AR Address

JL. DR. Wahidin No 68 D,

Registration Date

Nov 13, 2023

Expiry Date

Apr 18, 2028

Product Type

Diagnostic Ear, Nose and Throat Equipment

Acoustic chamber for audiometric testing.

Non Radiation Electromedics

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