NIDEK Auto Refractometer - Indonesia BPOM Medical Device Registration
NIDEK Auto Refractometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201411494. The device is manufactured by NIDEK CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULYA HUSADA JAYA.
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
NIDEK CO., LTD.Country of Origin
Japan
Authorized Representative
PT. MULYA HUSADA JAYAAR Address
JALAN KERINCI NO 2A
Registration Date
Jan 24, 2023
Expiry Date
Jun 06, 2027
Product Type
Diagnostic Eye Equipment
Ophthalmic refractometer.
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