SERENITY Mucus Extractor - Indonesia BPOM Medical Device Registration
SERENITY Mucus Extractor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903713034. The device is manufactured by JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
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 25, 2021
Expiry Date
Sep 18, 2025
Product Type
General Hospital Equipment and Other Individuals
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