GLIDESCOPE Titanium Video Laryngoscope Reusable - Indonesia BPOM Medical Device Registration

GLIDESCOPE Titanium Video Laryngoscope Reusable is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801024039. The device is manufactured by VERATHON MEDICAL (CANADA) ULC. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL MEDICAL PRESS.

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