SERENITY Nasal Oxygen Cannula - Indonesia BPOM Medical Device Registration
SERENITY Nasal Oxygen Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403712464. 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.
Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Mar 09, 2023
Expiry Date
Aug 25, 2025
Product Type
Therapeutic Anesthesia Equipment
Nasal oxygen cannula.
Non Electromedic Non Sterile
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