PENTAX Video Duodenoscope - Indonesia BPOM Medical Device Registration
PENTAX Video Duodenoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801220400. 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 PT. INDOMEDIK NIAGA PERKASA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HOYA CORPORATION PENTAX MIYAGI FACTORYCountry of Origin
Japan
Authorized Representative
PT. INDOMEDIK NIAGA PERKASAAR 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 12, 2024
Expiry Date
Jun 12, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Radiation Electromedics
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