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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.

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BPOM Registered
Risk Class Kelas Resiko : A
RMS Medical Flowmeter
Analysis ID: AKL 10402127962

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. RIKOWAN PROSPEROUS PROSPEROUS

AR 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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