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CLARITAS iRAD - Indonesia BPOM Medical Device Registration

CLARITAS iRAD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320758. The device is manufactured by CLARITAS HEALTHTECH PTE. LTD. from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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 : B
CLARITAS iRAD
Analysis ID: AKL 21501320758

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Feb 02, 2023

Expiry Date

Nov 25, 2027

Product Type

Diagnostic Radiology Equipment

Medical image management and processing system.

Non Radiation Electromedics

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