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Aqua Pure - Indonesia BPOM Medical Device Registration

Aqua Pure is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204420417. The device is manufactured by AVIZOR S.A. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALFA INTERNAL OPTINDO.

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
Aqua Pure
Analysis ID: AKL 21204420417

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

AVIZOR S.A.

Country of Origin

Spain

Authorized Representative

PT. ALFA INTERNAL OPTINDO

AR Address

JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001

Registration Date

Sep 02, 2024

Expiry Date

Feb 12, 2029

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens care products.

Non Electromedic Sterile

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