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OWANDY I-Max Ceph - Indonesia BPOM Medical Device Registration

OWANDY I-Max Ceph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20601320079. The device is manufactured by OWANDY RADIOLOGY from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REDOSCO PRANA DIPTA.

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 : C
OWANDY I-Max Ceph
Analysis ID: AKL 20601320079

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

OWANDY RADIOLOGY

Country of Origin

France

Authorized Representative

PT. REDOSCO PRANA DIPTA

AR Address

Wangsa Niaga Wetan N0.15, Komplek Kota Baru Parahyangan

Registration Date

Jul 11, 2023

Expiry Date

Mar 01, 2028

Product Type

Diagnostic Dental Equipment

Extraoral source x-ray system.

Electromedic Radiation

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