Glidescope Core System - Indonesia BPOM Medical Device Registration
Glidescope Core System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801320615. 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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Risk Classification
Product Class
Kelas : 2
Manufacturer
VERATHON MEDICAL (CANADA) ULC.Country of Origin
Canada
Authorized Representative
PT. GLOBAL MEDICAL PRESSAR Address
Jl. Raya Kebon Jeruk No.26 RT.011 RW.002, Kelurahan Kebon Jeruk, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta
Registration Date
Feb 13, 2024
Expiry Date
Nov 30, 2025
Product Type
Diagnostic Gastroenterology-Urology Equipment
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