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HEYER Respiratory Humidifier - Indonesia BPOM Medical Device Registration

HEYER Respiratory Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403121052. The device is manufactured by HEYER MEDICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FOR ANY MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
HEYER Respiratory Humidifier
Analysis ID: AKL 20403121052

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

FOR ANY MEDICAL INDONESIA

AR Address

Jalan RS Fatmawati (Fatmawati Grand Centre) Blok II Kavling Nomor 215 RT.003 RW.010

Registration Date

May 07, 2024

Expiry Date

Nov 28, 2028

Product Type

Therapeutic Anesthesia Equipment

Respiratory gas humidifier.

Non Radiation Electromedics

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DJ Fang

DJ Fang

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