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OmniAire 1600PAC - Indonesia BPOM Medical Device Registration

OmniAire 1600PAC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903910574. The device is manufactured by OMNITEC DESIGN, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRACE ETERNAL MEANS.

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
OmniAire 1600PAC
Analysis ID: AKL 20903910574

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. GRACE ETERNAL MEANS

AR Address

Rukan Mutiara Taman Palem A10/17 Cengkareng - Jakarta Barat

Registration Date

Mar 11, 2019

Expiry Date

Dec 31, 2023

Product Type

General Hospital Equipment and Other Individuals

Medical ultraviolet air purifier.

Non Radiation Electromedics

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