GENESYS MATRYX Interference Screw - Indonesia BPOM Medical Device Registration
GENESYS MATRYX Interference Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302911736. The device is manufactured by CONMED CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PETAN DAYA MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CONMED CORPORATIONCountry of Origin
United States
Authorized Representative
PETAN DAYA MEDICAAR Address
Komplek Setia Budi Point Jl. Setia Budi Blok C No. 3-4 Medan
Registration Date
Jul 28, 2022
Expiry Date
Dec 31, 2026
Product Type
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