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TOMEY Multifunction Unit - Indonesia BPOM Medical Device Registration

TOMEY Multifunction Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201915009. The device is manufactured by TOMEY CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA MEDICAL ABADI.

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
TOMEY Multifunction Unit
Analysis ID: AKL 21201915009

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TOMEY CORPORATION

Country of Origin

Japan

Authorized Representative

PT. MEGA MEDICAL ABADI

AR Address

Komplek Fatmawati Mas Blok B5 Kav. 207-208, Jl. RS. Fatmawati No. 20, RT. 005 RW. 010

Registration Date

Jun 06, 2024

Expiry Date

Apr 08, 2027

Product Type

Diagnostic Eye Equipment

Tonometer and accessories.

Non Radiation Electromedics

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