Pure Global

SAKAMED Manual Wheelchair 3 in 1 - Indonesia BPOM Medical Device Registration

SAKAMED Manual Wheelchair 3 in 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402914191. The device is manufactured by FOSHAN JUNNENG REHABILITATION EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SAKA UTAMA MEDIKA.

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 : A
SAKAMED Manual Wheelchair 3 in 1
Analysis ID: AKL 11402914191

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SAKA UTAMA MEDIKA

AR Address

JALAN GASEM PETING RAYA NO. 57

Registration Date

Jul 15, 2022

Expiry Date

Jul 13, 2025

Product Type

Prosthetic Physical Health Equipment

Mechanical wheelchair.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing