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NUBION NeoECG S120 - Indonesia BPOM Medical Device Registration

NUBION NeoECG S120 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220345. The device is manufactured by SHENZHEN CAREWELL ELECTRONICS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ASA PRATAMA PARTNERS.

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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BPOM Registered
Risk Class Kelas Resiko : B
NUBION NeoECG S120
Analysis ID: AKL 20502220345

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ASA PRATAMA PARTNERS

AR Address

MT Haryono Square No.OF 01/06 JL. MT.Haryono Kav.10, Kel. Bidara Cina , Kec. Jatinegara - Jakarta Timur

Registration Date

Oct 13, 2022

Expiry Date

May 08, 2025

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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