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SERENITY Compressor Nebulizer - Indonesia BPOM Medical Device Registration

SERENITY Compressor Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403712835. The device is manufactured by HONSUN (NANTONG) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY INDONESIA.

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
SERENITY Compressor Nebulizer
Analysis ID: AKL 20403712835

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SERENITY INDONESIA

AR Address

Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter

Registration Date

Sep 06, 2021

Expiry Date

Sep 06, 2026

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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DJ Fang

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