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HUNTLEIGH Sonicaid Team 3 - Indonesia BPOM Medical Device Registration

HUNTLEIGH Sonicaid Team 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101320094. 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 ESA MEDIKA MANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : B
HUNTLEIGH Sonicaid Team 3
Analysis ID: AKL 21101320094

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

ESA MEDIKA MANDIRI

AR Address

ESA 8 Building, 10th Floor, Jl. Ir. Soekarno Kavling 3-5

Registration Date

Aug 01, 2023

Expiry Date

Feb 22, 2027

Product Type

Obstetric and Gynecological Monitoring Equipment

Fetal cardiac monitor.

Non Radiation Electromedics

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