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PUREMEDIC Fetal Monitor - Indonesia BPOM Medical Device Registration

PUREMEDIC Fetal Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101420027. The device is manufactured by SHENZEN JUMPER MEDICAL EQUIPMENT CO. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.

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
PUREMEDIC Fetal Monitor
Analysis ID: AKL 21101420027

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ALKESTRON SELF-SOURCE

AR Address

Komplek Ruko Griya Inti Sentosa, JI. Griya Agung Blok O No.95, RT.2/RW.20

Registration Date

May 21, 2024

Expiry Date

Sep 06, 2026

Product Type

Obstetric and Gynecological Monitoring Equipment

Fetal cardiac monitor.

Non Radiation Electromedics

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