Pure Global

PUREMED Anti Decubitus Mattress With Pump - Indonesia BPOM Medical Device Registration

PUREMED Anti Decubitus Mattress With Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902819190. The device is manufactured by SHENZHEN FITCONN TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ROYAL SEJAHTERA MANDIRI.

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
PUREMED Anti Decubitus Mattress With Pump
Analysis ID: AKL 20902819190

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ROYAL SEJAHTERA MANDIRI

AR Address

Ruko Mahkota Ancol Blok E No.53, Jl. RE Martadinata, Kelurahan Pademanagn Barat

Registration Date

Sep 06, 2021

Expiry Date

Sep 06, 2024

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
Other Products from ROYAL SEJAHTERA MANDIRI
Products with the same authorized representative (1 products)