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PHILIPS MobileDiagnost wDR - Indonesia BPOM Medical Device Registration

PHILIPS MobileDiagnost wDR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501211604. The device is manufactured by SEDECAL. from Spain, 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.

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Risk Class Kelas Resiko : C
PHILIPS MobileDiagnost wDR
Analysis ID: AKL 21501211604

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SEDECAL.

Country of Origin

Spain

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

Nov 08, 2021

Expiry Date

Sep 20, 2026

Product Type

Diagnostic Radiology Equipment

Mobile x-ray system.

Electromedic Radiation

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