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LUTECH Multi-parameter Patient Monitor - Indonesia BPOM Medical Device Registration

LUTECH Multi-parameter Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502122170. The device is manufactured by LUTECH INDUSTRIES, INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GAMAMED.

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BPOM Registered
Risk Class Kelas Resiko : B
LUTECH Multi-parameter Patient Monitor
Analysis ID: AKL 20502122170

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

GAMAMED

AR Address

JL. WR. SUPRATMAN 56 B

Registration Date

Apr 16, 2021

Expiry Date

Nov 28, 2023

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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