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FAMILY DR. Nasal Dilator - Indonesia BPOM Medical Device Registration

FAMILY DR. Nasal Dilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702420053. The device is manufactured by DREAM AIR CO. LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOCORE PERKASA.

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 : A
FAMILY DR. Nasal Dilator
Analysis ID: AKL 10702420053

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DREAM AIR CO. LTD.

Country of Origin

Korea

Authorized Representative

PT. INDOCORE PERKASA

AR Address

Komplek Graha Mas Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006

Registration Date

Jul 05, 2024

Expiry Date

Feb 06, 2029

Product Type

Prosthetic Ear, Nose and Throat Equipment

Nasal dilator.

Non Electromedic Non Sterile

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