GENADYNE Negative Pressure Wound Therapy - Indonesia BPOM Medical Device Registration
GENADYNE Negative Pressure Wound Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603917465. The device is manufactured by GENADYNE BIOTECHNOLOGIES, INC., USA from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GENADYNE BIOTECHNOLOGIES, INC., USACountry of Origin
United States
Authorized Representative
SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
Feb 01, 2024
Expiry Date
May 23, 2028
Product Type
Surgical Equipment
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