VITROLIFE Pasteur Pipette - Indonesia BPOM Medical Device Registration

VITROLIFE Pasteur Pipette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105420034. The device is manufactured by VITROLIFE SWEDEN AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PHARMALAB INTERSAINS.

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