SCHOLLY Light Guide and Adapter - Indonesia BPOM Medical Device Registration
SCHOLLY Light Guide and Adapter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703220101. The device is manufactured by SCHOLLY FIBEROPTIC GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SCHOLLY FIBEROPTIC GMBH.Country of Origin
Germany
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Dec 23, 2022
Expiry Date
Mar 30, 2026
Product Type
Ear, Nose and Throat Surgical Equipment
Ear, nose, and throat fiberoptic light source and carrier.
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