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HUNTLEIGH Sonicaid Encore Fetal/Maternal Monitor - Indonesia BPOM Medical Device Registration

HUNTLEIGH Sonicaid Encore Fetal/Maternal Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101917698. The device is manufactured by HUNTLEIGH HEALTHCARE LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BETA MEDICAL.

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BPOM Registered
Risk Class Kelas Resiko : B
HUNTLEIGH Sonicaid Encore Fetal/Maternal Monitor
Analysis ID: AKL 21101917698

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

BETA MEDICAL

AR Address

Jl. Pangeran Antasari No. 212

Registration Date

Nov 29, 2019

Expiry Date

Jan 14, 2024

Product Type

Obstetric and Gynecological Monitoring Equipment

Fetal cardiac monitor.

Non Radiation Electromedics

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