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RADIFOCUS Torque Device - Indonesia BPOM Medical Device Registration

RADIFOCUS Torque Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321033. The device is manufactured by TERUMO MEDICAL PRODUCTS (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TERUMO INDONESIA.

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
RADIFOCUS Torque Device
Analysis ID: AKL 20501321033

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

Sep 26, 2023

Expiry Date

Jul 12, 2028

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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