Pure Global

DREAMWEAR Full Face Mask - Indonesia BPOM Medical Device Registration

DREAMWEAR Full Face Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403025563. The device is manufactured by PHILIPS VOLCANO CORPORATION VOLCARICA S.R.L. from Costa Rica, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
DREAMWEAR Full Face Mask
Analysis ID: AKL 10403025563

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Costa Rica

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005

Registration Date

Dec 20, 2024

Expiry Date

Oct 30, 2029

Product Type

Therapeutic Anesthesia Equipment

Oxygen mask.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing