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TAKAGI Mobile Slitlamp - Indonesia BPOM Medical Device Registration

TAKAGI Mobile Slitlamp is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201320327. The device is manufactured by TAKAGI SEIKO, CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SURYA TAMA MEDIKA.

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
TAKAGI Mobile Slitlamp
Analysis ID: AKL 21201320327

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

SURYA TAMA MEDIKA

AR Address

Jl m hasibuan ruko suncity pbb. 37 real blok e.27 rt 004 rw 002 kel margajaya kec bekasi selatan kota bekasi

Registration Date

Jun 11, 2023

Expiry Date

Nov 16, 2027

Product Type

Diagnostic Eye Equipment

AC-powered slitlamp biomicroscope.

Non Radiation Electromedics

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