ZEISS FORUM - Indonesia BPOM Medical Device Registration
ZEISS FORUM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321051. The device is manufactured by CARL ZEISS MEDITEC AG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CARL ZEISS NEW ZEISS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARL ZEISS MEDITEC AGCountry of Origin
Germany
Authorized Representative
PT. CARL ZEISS NEW ZEISSAR Address
ARKADIA GREEN PARK, TOWER C, LANTAI 12, JL. TB SIMATUPANG KAV. 88
Registration Date
Jul 27, 2023
Expiry Date
Sep 30, 2026
Product Type
Diagnostic Radiology Equipment
Medical image management and processing system.
Non Radiation Electromedics
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AT TORBI 709
AT LISA tri toric 939
ZEISS KINEVO 900
ZEISS RESCAN 700
AT TORBI 719
ARTEVO 800
QUATERA 700
OPMI DRAPES Sterile
ZEISS IOLMaster 500
AT LISA tri 839MP
CARL ZEISS MEDITEC AG
AT LISA tri 839MP
CARL ZEISS MEDITEC SAS
AT TORBI 709
CARL ZEISS MEDITEC SAS
AT LISA tri toric 939
CARL ZEISS MEDITEC SAS
AT TORBI 719
CARL ZEISS MEDITEC SAS
AT TORBI 709
CARL ZEISS MEDITEC AG
AT LISA tri toric 939
CARL ZEISS MEDITEC AG
ZEISS KINEVO 900
CARL ZEISS MEDITEC AG
ZEISS RESCAN 700
CARL ZEISS MEDITEC AG
AT LISA tri toric 949
CARL ZEISS MEDITEC AG (BERLIN)