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VISUPHOR 500 - Indonesia BPOM Medical Device Registration

VISUPHOR 500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201220131. The device is manufactured by HUVITZ CO. LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is CARL ZEISS NEW ZEISS.

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
VISUPHOR 500
Analysis ID: AKL 11201220131

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

HUVITZ CO. LTD.

Country of Origin

Korea

Authorized Representative

CARL ZEISS NEW ZEISS

AR Address

CARL ZEISS INDONESIA

Registration Date

Aug 11, 2022

Expiry Date

Sep 30, 2026

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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