GENADYNE Nanogen Actigel - Indonesia BPOM Medical Device Registration
GENADYNE Nanogen Actigel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420799. The device is manufactured by GENADYNE BIOTECHNOLOGIES, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SEKARGUNA MEDIKA.
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GENADYNE Nanogen Aktigel
Risk Classification
Product Class
Kelas : 2
Manufacturer
GENADYNE BIOTECHNOLOGIES, INC.Country of Origin
United States
Authorized Representative
SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
Apr 06, 2024
Expiry Date
May 23, 2028
Product Type
Surgical Equipment
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