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ONEMED Bubble Mattress with Pump / Alternating Pressure Mattress - Indonesia BPOM Medical Device Registration

ONEMED Bubble Mattress with Pump / Alternating Pressure Mattress is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902913858. The device is manufactured by GUANGDONG YUEHUA MEDICAL INSTRUMENT FACTORY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTISUMBER HASILSEMPURNA.

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
ONEMED Bubble Mattress with Pump / Alternating Pressure Mattress
Analysis ID: AKL 20902913858

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INTISUMBER HASILSEMPURNA

AR Address

KOMPLEK DARMO PARK II BLOK IV NO. 14-15 JL. MAYJEND SUNGKONO SURABAYA

Registration Date

Dec 22, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic General and Individual Hospital Equipment

Alternating pressure air flotation mattress.

Non Radiation Electromedics

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