ZEISS Digital Lens SmartLife PRO Individual, index 1.50 - Indonesia BPOM Medical Device Registration
ZEISS Digital Lens SmartLife PRO Individual, index 1.50 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204220538. The device is manufactured by CARL ZEISS VISION TECHNOLOGIES (GUANGZHOU) LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is VARIOUS ETERNAL GIFTS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CARL ZEISS VISION TECHNOLOGIES (GUANGZHOU) LTD.Country of Origin
China
Authorized Representative
VARIOUS ETERNAL GIFTSAR Address
Ruko Taman Galaxy, Jl. Nusa Indah Raya Blok W No.1A Kel. Jakasetia, Kec. Bekasi Selatan, Kota Bekasi, Jawa Barat
Registration Date
Dec 30, 2022
Expiry Date
Sep 30, 2025
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
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