RMS Medical Flowmeter - Indonesia BPOM Medical Device Registration
RMS Medical Flowmeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402127962. The device is manufactured by NANJING OCEAN MEDICAL PRODUCTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. RIKOWAN PROSPEROUS PROSPEROUS.
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
NANJING OCEAN MEDICAL PRODUCTS CO., LTD.Country of Origin
China
Authorized Representative
PT. RIKOWAN PROSPEROUS PROSPEROUSAR Address
Jl. Mangga Dua Raya Komplek Ruko Harco Mangga Dua Plaza Blok K/30, Mangga Dua Selatan
Registration Date
Dec 17, 2021
Expiry Date
Dec 16, 2024
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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