Pure Global

SERENITY Sterilizer Cupboard - Indonesia BPOM Medical Device Registration

SERENITY Sterilizer Cupboard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903310962. The device is manufactured by GUANGDONG KONSE ELECTRICAL APPLIANCE CO., LTD., P.R. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
SERENITY Sterilizer Cupboard
Analysis ID: AKL 20903310962

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

Nov 16, 2022

Expiry Date

Apr 06, 2027

Product Type

General Hospital Equipment and Other Individuals

Steam sterilizer.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing