GEA Penlight - Indonesia BPOM Medical Device Registration
GEA Penlight is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903918414. The device is manufactured by WENZHOU YI HONG MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
WENZHOU YI HONG MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Sep 30, 2022
Expiry Date
Sep 29, 2025
Product Type
General Hospital Equipment and Other Individuals
Battery-powered medical examination light.
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