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MD SCOPE Video Otoscope - Indonesia BPOM Medical Device Registration

MD SCOPE Video Otoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703320270. The device is manufactured by APPLE BIOMEDICAL INC. from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MULTISERA INDOSA.

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
MD SCOPE Video Otoscope
Analysis ID: AKL 10703320270

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Taiwan (China)

Authorized Representative

MULTISERA INDOSA

AR Address

Jl. Jend. Sudirman No. 689 RT 21 RW 007

Registration Date

Oct 28, 2024

Expiry Date

Oct 09, 2029

Product Type

Ear, Nose and Throat Surgical Equipment

Otoscope.

Non Radiation Electromedics

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