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DECANAV Electrophysiology Catheter - Indonesia BPOM Medical Device Registration

DECANAV Electrophysiology Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501411005. The device is manufactured by BIOSENSE WEBSTER, INC. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JOHNSON & JOHNSON NEW ZEALAND.

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BPOM Registered
Risk Class Kelas Resiko : C
DECANAV Electrophysiology Catheter
Analysis ID: AKL 20501411005

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. JOHNSON & JOHNSON NEW ZEALAND

AR Address

K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A

Registration Date

Sep 14, 2021

Expiry Date

Sep 02, 2025

Product Type

Diagnostic Cardiology Equipment

Electrode recording catheter or electrode recording probe.

Non Electromedic Sterile

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