GENADYNE Nanogen Active - Indonesia BPOM Medical Device Registration
GENADYNE Nanogen Active is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603324865. The device is manufactured by GENADYNE BIOTECHNOLOGIES, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEKARGUNA MEDIKA.
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GENADYNE Nanogen Aktiv
Risk Classification
Product Class
Kelas : 1
Manufacturer
GENADYNE BIOTECHNOLOGIES, INC.Country of Origin
United States
Authorized Representative
SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
Aug 31, 2023
Expiry Date
May 22, 2028
Product Type
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