PUREMED Penlight - Indonesia BPOM Medical Device Registration
PUREMED Penlight is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903815050. 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. ROYAL SEJAHTERA MANDIRI.
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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. ROYAL SEJAHTERA MANDIRIAR Address
RUKO MAHKOTA ANCOL BLOK E NO. 53 JL. RE MARTADINATA KEL. PADEMANGAN BARAT
Registration Date
Jan 22, 2021
Expiry Date
Jan 21, 2024
Product Type
General Hospital Equipment and Other Individuals
Battery-powered medical examination light.
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