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AMBU NEUROLINE 710 - Indonesia BPOM Medical Device Registration

AMBU NEUROLINE 710 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001612126. The device is manufactured by AMBU SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAVINDRA PUTRAPRATAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
AMBU NEUROLINE 710
Analysis ID: AKL 21001612126

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AMBU SDN. BHD.

Country of Origin

Malaysia

Authorized Representative

PT. RAVINDRA PUTRAPRATAMA

AR Address

Pusat Niaga Duta Mas Fatmawati Blok B2-18. Jl. Fatmawati 39 - Cipete Utara Jakarta 12150

Registration Date

Oct 18, 2024

Expiry Date

Mar 31, 2027

Product Type

Diagnostic Neurology Equipment

Needle electrode.

Non Electromedic Sterile

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