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SZOSEN Suffered Monitor - Indonesia BPOM Medical Device Registration

SZOSEN Suffered Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502027749. The device is manufactured by SHENZHEN OSEN TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CIPTA MEDIKA INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Risk Class Kelas Resiko : B
SZOSEN Suffered Monitor

SZOSEN Patien Monitor

Analysis ID: AKL 20502027749

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

CIPTA MEDIKA INDONESIA

AR Address

GRAND UNEDO JL. BINA MARGA NO. 94 G

Registration Date

Dec 15, 2020

Expiry Date

Aug 14, 2025

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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