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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
HUVITZ CO. LTD.Country of Origin
Korea
Authorized Representative
CARL ZEISS NEW ZEISSAR Address
CARL ZEISS INDONESIA
Registration Date
Aug 11, 2022
Expiry Date
Sep 30, 2026
Product Type
Diagnostic Eye Equipment
Ophthalmic refractometer.
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