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FUKUDA DENSHI Sphygmomanometer & Sphygmograph - Indonesia BPOM Medical Device Registration

FUKUDA DENSHI Sphygmomanometer & Sphygmograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501711945. The device is manufactured by FUKUDA DENSHI CO., LTD SHIROI FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
FUKUDA DENSHI Sphygmomanometer & Sphygmograph
Analysis ID: AKL 20501711945

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Mar 06, 2021

Expiry Date

Mar 31, 2025

Product Type

Diagnostic Cardiology Equipment

Noninvasive blood pressure measurement system.

Non Radiation Electromedics

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