PUTTI ATTI Teether - Indonesia BPOM Medical Device Registration

PUTTI ATTI Teether is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10604420024. The device is manufactured by LEE & LEE HI-TECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ROYAL MITRA PRATAMA.

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