SERENITY Medical Oxygen Regulator - Indonesia BPOM Medical Device Registration
SERENITY Medical Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402710065. The device is manufactured by YUYAO YUFENG MEDICAL EQUIPMENT CO. LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
YUYAO YUFENG MEDICAL EQUIPMENT CO. LTD.Country of Origin
China
Authorized Representative
SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Nov 07, 2021
Expiry Date
Oct 21, 2026
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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