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CORONA Compressor Nebulizer - Indonesia BPOM Medical Device Registration

CORONA Compressor Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403111358. The device is manufactured by JIANGSU FOLEE MEDICAL EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIMA UTAMA CIPTA NIAGA.

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
CORONA Compressor Nebulizer
Analysis ID: AKL 20403111358

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PRIMA UTAMA CIPTA NIAGA

AR Address

JL. PLUIT KARANG SARI BLOK D7 T NO.72 MUARA KARANG - JAKARTA UTARA

Registration Date

Nov 15, 2018

Expiry Date

Nov 16, 2023

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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