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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
G.W. PLASTICS TUCSONCountry of Origin
United States
Authorized Representative
PHILIPS INDONESIA COMMERCIALAR 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
TRILOGY EV300
RESPIRONICS INC.
PHILIPS CT 5300
PHILIPS HEALTHCARE (SUZHOU) CO., LTD.
PHILIPS CT 5300
PHILIPS HEALTHCARE (SUZHOU) CO., LTD.
PHILIPS IntelliVue Active Display AD85
PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH
PHILIPS IntelliSite Pathology Solution
Philips Medical Systems Nederland B.V.
PHILIPS IntelliVue XDS Software
PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH.
PHILIPS IntelliVue Guardian Software
PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH.
PHILIPS CT 5300
PHILIPS HEALTHCARE (SUZHOU) CO., LTD.
PHILIPS CT 5300
PHILIPS HEALTHCARE (SUZHOU) CO., LTD.
EPIQ 5 Diagnostic Ultrasound System
PHILIPS ULTRASOUND, LLC.

