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GLOREHA AIR - Indonesia BPOM Medical Device Registration

GLOREHA AIR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403220316. The device is manufactured by IDROGENET S.R.L from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is POLARIS ALKES STARINDO.

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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Risk Class Kelas Resiko : A
GLOREHA AIR

GLOREHA ARIA

Analysis ID: AKL 11403220316

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

IDROGENET S.R.L

Country of Origin

Italy

Authorized Representative

POLARIS ALKES STARINDO

AR Address

JL. Gunung Sahari Raya No. 12 G Gunung Sahari Utara, Sawah Besar

Registration Date

Oct 31, 2022

Expiry Date

Jun 01, 2025

Product Type

Therapeutic Physical Health Equipment

Powered finger exerciser.

Non Radiation Electromedics

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