Pure Global

APEX Alternating Pressure Relief System - Indonesia BPOM Medical Device Registration

APEX Alternating Pressure Relief System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420018. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
APEX Alternating Pressure Relief System
Analysis ID: AKL 20902420018

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 No. 89 KM. 45,5, Kode Pos 17530, Desa/Kelurahan Sukadanau, Kec. Cikarang Barat, Kab. Bekasi, Prov. Jawa Barat

Registration Date

Jan 05, 2024

Expiry Date

Aug 24, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Alternating pressure air flotation mattress.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing