PRIMUS 200 - Indonesia BPOM Medical Device Registration
PRIMUS 200 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201220218. The device is manufactured by CARL ZEISS SUZHOU CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CARL ZEISS NEW ZEISS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARL ZEISS SUZHOU CO., LTD.Country of Origin
China
Authorized Representative
CARL ZEISS NEW ZEISSAR Address
CARL ZEISS INDONESIA
Registration Date
Dec 05, 2022
Expiry Date
Jan 01, 2026
Product Type
Diagnostic Eye Equipment
Optical Coherence Tomography
Non Radiation Electromedics
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