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ONEHEALTH Air Mattress - Indonesia BPOM Medical Device Registration

ONEHEALTH Air Mattress is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902128891. The device is manufactured by GUANGDONG KAIYANG MEDICAL TECHNOLOGY GROUP CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDICAL ERA ALKESINDO.

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
ONEHEALTH Air Mattress
Analysis ID: AKL 20902128891

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MEDICAL ERA ALKESINDO

AR Address

Jl. Sisingamangaraja Kilometer 10.8, Komplek Amplas Trade Centre Blok Mahoni nomor 08, Kota Medan, Provinsi Sumatera Utara, Kode Pos: 20148

Registration Date

Nov 28, 2024

Expiry Date

Nov 27, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Alternating pressure air flotation mattress.

Non Radiation Electromedics

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