PIGEON Teether Step 2 - Indonesia BPOM Medical Device Registration

PIGEON Teether Step 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10604906521. The device is manufactured by PIGEON CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTI INDOCITRA. TBK.

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