CRYOPEN O+ - Indonesia BPOM Medical Device Registration

CRYOPEN O+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325623. The device is manufactured by H&O EQUIPMENTS NV/SA from Belgium, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is REDO MARKETING INDONESIA.

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