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INTER Patient Monitor - Indonesia BPOM Medical Device Registration

INTER Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220164. The device is manufactured by UTECH CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AMBRA ANUBAWA BERSAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
INTER Patient Monitor
Analysis ID: AKL 20502220164

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

UTECH CO.,LTD

Country of Origin

China

Authorized Representative

PT. AMBRA ANUBAWA BERSAMA

AR Address

JI. KIhajar Dewantara Ruko Golden 8 Blok A. No. 7 Gading Serpong Summarecon Tangerang Banten 15810 Tlp. 021. 29238848

Registration Date

May 19, 2022

Expiry Date

May 18, 2025

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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