AURORA Operation Shadowless Lamp - Indonesia BPOM Medical Device Registration
AURORA Operation Shadowless Lamp is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603718034. The device is manufactured by SHENGDA MEDICAL DEVICE FACTORY. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GEBANG SURYA HARAPAN.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENGDA MEDICAL DEVICE FACTORY.Country of Origin
China
Authorized Representative
PT. GEBANG SURYA HARAPANAR Address
Ruko Puri Botanical Junction Blok I 10 No. 1 Jl. Raya Joglo RT 007 RW 001 Kel. Joglo, Kec. Kembangan, Jakarta Barat
Registration Date
Nov 26, 2020
Expiry Date
Nov 10, 2023
Product Type
Surgical Equipment
Surgical lamp.
Non Radiation Electromedics
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