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APEX Heated Humidifier - Indonesia BPOM Medical Device Registration

APEX Heated Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403514510. The device is manufactured by APEX MEDICAL CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PROTECHMA 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 : B
APEX Heated Humidifier
Analysis ID: AKL 20403514510

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

APEX MEDICAL CORP.

Country of Origin

Taiwan (China)

Authorized Representative

PT. PROTECHMA INDONESIA

AR Address

Jl. Teuku Umar KM 45,5 No.89 Cibitung Bekasi, Jawa Barat Telp : 021-88326735 Fax : 021-88328007

Registration Date

May 03, 2019

Expiry Date

Jan 01, 2024

Product Type

Therapeutic Anesthesia Equipment

Therapeutic humidifier for home use.

Non Radiation Electromedics

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