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MAICO Tympanometer - Indonesia BPOM Medical Device Registration

MAICO Tympanometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701715295. The device is manufactured by MAICO DIAGNOSTICS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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
MAICO Tympanometer
Analysis ID: AKL 20701715295

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

Nov 23, 2022

Expiry Date

Sep 13, 2025

Product Type

Diagnostic Ear, Nose and Throat Equipment

Auditory impedance tester.

Non Radiation Electromedics

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