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GP Care Guedel Airway - Indonesia BPOM Medical Device Registration

GP Care Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403120188. The device is manufactured by HAIYAN KANGYUAN MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GLOBAL PHARMA INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
GP Care Guedel Airway
Analysis ID: AKL 10403120188

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. GLOBAL PHARMA INDONESIA

AR Address

PERGUDANGAN LIO BARU ASRI Jl. Bouraq Lio Baru Blok C1 No. 33 RT 004 RW 01, Batusari, Batuceper

Registration Date

Jan 12, 2021

Expiry Date

Jan 11, 2024

Product Type

Therapeutic Anesthesia Equipment

Oropharyngeal airway

Non Electromedic Sterile

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