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FAMILY DR. ™ FETAL DOPPLER AD51F - Indonesia BPOM Medical Device Registration

FAMILY DR. ™ FETAL DOPPLER AD51F is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320901. The device is manufactured by HUNAN ACCURATE BIO-MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOCORE PERKASA.

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BPOM Registered
Risk Class Kelas Resiko : B
FAMILY DR. ™ FETAL DOPPLER AD51F
Analysis ID: AKL 21501320901

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOCORE PERKASA

AR Address

Komplek Graha Mas Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006 Kel. Jati, Kec. Pulo Gadung, Jakarta Timur, DKI Jakarta

Registration Date

Apr 18, 2023

Expiry Date

Oct 12, 2027

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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