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AGILIS HISPRO™ Steerable Catheter With Electrodes - Indonesia BPOM Medical Device Registration

AGILIS HISPRO™ Steerable Catheter With Electrodes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501123382. The device is manufactured by ST JUDE MEDICAL from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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Risk Class Kelas Resiko : C
AGILIS HISPRO™ Steerable Catheter With Electrodes
Analysis ID: AKL 20501123382

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ST JUDE MEDICAL

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5

Registration Date

Aug 31, 2021

Expiry Date

Jun 26, 2025

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

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