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PENTAX Medical Ultrasound Video Bronchoscope - Indonesia BPOM Medical Device Registration

PENTAX Medical Ultrasound Video Bronchoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420157. The device is manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOMEDIK NIAGA PERKASA.

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BPOM Registered
Risk Class Kelas Resiko : B
PENTAX Medical Ultrasound Video Bronchoscope
Analysis ID: AKL 20801420157

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

INDOMEDIK NIAGA PERKASA

AR Address

JALAN RAYA KEBAYORAN LAMA NO.35 RT.008 RW.001 Kel. Sukabumi Selatan Kec, Kebon Jeruk, Jakarta Barat, provinsi DKI Jakarta

Registration Date

Apr 23, 2024

Expiry Date

Sep 11, 2026

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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