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OptiChamber Diamond - Indonesia BPOM Medical Device Registration

OptiChamber Diamond is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403122739. The device is manufactured by G.W. PLASTICS TUCSON from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHILIPS INDONESIA COMMERCIAL.

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
OptiChamber Diamond
Analysis ID: AKL 20403122739

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

May 09, 2021

Expiry Date

Sep 18, 2025

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Electromedic Non Sterile

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