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SERENITY Non-Rebreathing Mask - Indonesia BPOM Medical Device Registration

SERENITY Non-Rebreathing Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403713617. The device is manufactured by JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. 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 : A
SERENITY Non-Rebreathing Mask
Analysis ID: AKL 10403713617

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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

Dec 15, 2021

Expiry Date

Aug 25, 2025

Product Type

Therapeutic Anesthesia Equipment

Nonrebreathing mask.

Non Electromedic Sterile

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