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FUKUDA Sangyo Spiroanalyzer - Indonesia BPOM Medical Device Registration

FUKUDA Sangyo Spiroanalyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401913067. The device is manufactured by FUKUDA SANGYO. CO. LTD., TAKATA FACTORY. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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BPOM Registered
Risk Class Kelas Resiko : B
FUKUDA Sangyo Spiroanalyzer
Analysis ID: AKL 20401913067

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. ENSEVAL MEDIKA PRIMA

AR Address

JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG

Registration Date

Aug 07, 2021

Expiry Date

Jul 08, 2026

Product Type

Diagnostic Anesthesia Equipment

Diagnostic spirometer.

Non Radiation Electromedics

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