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AQUABPLUS - Indonesia BPOM Medical Device Registration

AQUABPLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805020779. The device is manufactured by VIVONIC GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS MEDICAL CARE INDONESIA.

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 : C
AQUABPLUS
Analysis ID: AKL 20805020779

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

VIVONIC GMBH

Country of Origin

Germany

Authorized Representative

PT. FRESENIUS MEDICAL CARE INDONESIA

AR Address

Tempo Scan Tower, Lt. 20, Jl. H.R. Rasuna Said Kav. 3-4

Registration Date

Aug 07, 2024

Expiry Date

Feb 04, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Water purification system for hemodialysis.

Non Radiation Electromedics

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