ZUMAX DFK Loupes - Indonesia BPOM Medical Device Registration
ZUMAX DFK Loupes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204420159. The device is manufactured by ZUMAX MEDICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is THOMASONG NIRMALA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ZUMAX MEDICAL CO., LTDCountry of Origin
China
Authorized Representative
THOMASONG NIRMALAAR Address
Jl. AM. Sangaji No. 20A
Registration Date
Apr 05, 2024
Expiry Date
Dec 30, 2026
Product Type
Therapeutic Eye Equipment
Low-power binocular loupe.
Non Electromedic Non Sterile
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