PHILIPS XPERCT DUAL - Indonesia BPOM Medical Device Registration
PHILIPS XPERCT DUAL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501715752. The device is manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Country of Origin
Netherlands
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Nov 21, 2023
Expiry Date
Feb 05, 2026
Product Type
Diagnostic Radiology Equipment
Medical image management and processing system.
Non Radiation Electromedics
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