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MEDINA Alternating Pressure Matress with Pump - Indonesia BPOM Medical Device Registration

MEDINA Alternating Pressure Matress with Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902026485. The device is manufactured by XIAMEN SENYANG CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDINA TECHNIQUE 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
MEDINA Alternating Pressure Matress with Pump
Analysis ID: AKL 20902026485

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDINA TECHNIQUE ALKESINDO

AR Address

Rukan Puri Mansion Blok A No. 28 Jl. Lingkar Luar Barat

Registration Date

Jul 13, 2023

Expiry Date

Jul 11, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Alternating pressure air flotation mattress.

Non Radiation Electromedics

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