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KENZMEDICO Aneroid Sphygmomanometer - 540 - Indonesia BPOM Medical Device Registration

KENZMEDICO Aneroid Sphygmomanometer - 540 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501616018. The device is manufactured by KENZMEDICO CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
KENZMEDICO Aneroid Sphygmomanometer - 540
Analysis ID: AKL 20501616018

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Nov 06, 2020

Expiry Date

Sep 28, 2025

Product Type

Diagnostic Cardiology Equipment

Noninvasive blood pressure measurement system.

Non Electromedic Non Sterile

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