ZEISS Resight - Indonesia BPOM Medical Device Registration
ZEISS Resight is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422498. The device is manufactured by CARL ZEISS MEDITEC AG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CARL ZEISS NEW ZEISS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CARL ZEISS MEDITEC AG.Country of Origin
Germany
Authorized Representative
PT. CARL ZEISS NEW ZEISSAR Address
Arkadia Green Park, Tower G 16th Floor, Suite 1608 Jalan TB. Simatupang Kavling 88
Registration Date
Oct 22, 2024
Expiry Date
Sep 30, 2029
Product Type
Surgical Equipment
Surgical microscope and accessories.
Non Electromedic Non Sterile
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