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ProKnow DS - Indonesia BPOM Medical Device Registration

ProKnow DS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420954. The device is manufactured by ELEKTA SOLUTIONS AB from Sweden, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ELEKTA MEDICAL SOLUTIONS.

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
ProKnow DS
Analysis ID: AKL 21501420954

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

ELEKTA MEDICAL SOLUTIONS

AR Address

South Quarter Tower B, Lantai 11 unit B, Jalan R.A Kartini Kavling 8

Registration Date

Dec 30, 2024

Expiry Date

Aug 21, 2029

Product Type

Diagnostic Radiology Equipment

Medical image management and processing system.

Non Radiation Electromedics

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