RODENSTOCK Auto Refractometer - Indonesia BPOM Medical Device Registration
RODENSTOCK Auto Refractometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201917788. The device is manufactured by SHANGHAI SUPORE INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALFA INTERNAL OPTINDO.
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
SHANGHAI SUPORE INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
PT. ALFA INTERNAL OPTINDOAR Address
JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001
Registration Date
May 15, 2024
Expiry Date
Jan 01, 2029
Product Type
Diagnostic Eye Equipment
Ophthalmic refractometer.
Non Radiation Electromedics
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SUPORE Chart Projector
SUPORE Chart Projector
SUPORE View Tester / Phoroptor (electric)
SUPORE VT-8 Phoroptor (manual)
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Aqua Pure
AVIZOR S.A.
MENICARE Plus Multipurpose Solution
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MENIFOCAL Z
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MENICON Starter Kit for RGP Lenses
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SUPORE Trial Lens
SHANGHAI SUPORE INSTRUMENTS CO., LTD.
RODENSTOCK Pupilometer
SHANGHAI SUPORE INSTRUMENTS CO., LTD.
RODENSTOCK ACP-100 Compact Chart
SHANGHAI SUPORE INSTRUMENTS CO., LTD.

