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GLIDESCOPE AVL Video Laryngoscope - Indonesia BPOM Medical Device Registration

GLIDESCOPE AVL Video Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801026770. 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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BPOM Registered
Risk Class Kelas Resiko : B
GLIDESCOPE AVL Video Laryngoscope
Analysis ID: AKL 20801026770

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Canada

Authorized Representative

PT. GLOBAL MEDICAL PRESS

AR Address

Jl. Raya Kebon Jeruk No.26 RT.011 RW.002, Kelurahan Kebon Jeruk, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta

Registration Date

Feb 24, 2023

Expiry Date

Nov 30, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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