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CANON FULL AUTO REF-KERATOMETER - Indonesia BPOM Medical Device Registration

CANON FULL AUTO REF-KERATOMETER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201810486. The device is manufactured by CANON COMPONENTS from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRIUMPHANT MANDARIN OPTO-MEDIC.

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
CANON FULL AUTO REF-KERATOMETER
Analysis ID: AKL 11201810486

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

CANON COMPONENTS

Country of Origin

Japan

Authorized Representative

PT. TRIUMPHANT MANDARIN OPTO-MEDIC

AR Address

Jl. Senen Raya No. 135 Ruko Atrium Blok C No. 15 Jakarta Pusat 10410 Tlp : 021-3515478, 3516018 Fax : 021-3511606

Registration Date

Oct 12, 2022

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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