HOSPITECH Mucus Extractor - Indonesia BPOM Medical Device Registration
HOSPITECH Mucus Extractor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903110984. The device is manufactured by HOSPITECH MANUFACTURING SERVICES SDN., BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SCINTILLATING ASIAN CENTER.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HOSPITECH MANUFACTURING SERVICES SDN., BHD.Country of Origin
Malaysia
Authorized Representative
SCINTILLATING ASIAN CENTERAR Address
JL. Pantai Indah Barat, Komplek TOHO Pantai Indah Kapuk Blok H 25 & 27, Kamal Muara - Penjaringan Jakarta Utara
Registration Date
Aug 04, 2021
Expiry Date
Feb 01, 2026
Product Type
General Hospital Equipment and Other Individuals
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