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PENTAX Medical Video Colonoscope - Indonesia BPOM Medical Device Registration

PENTAX Medical Video Colonoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801520050. 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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
PENTAX Medical Video Colonoscope
Analysis ID: AKL 20801520050

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

Feb 08, 2025

Expiry Date

Jun 24, 2027

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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