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LASSO Electrophysiology Catheter With Auto ID - Indonesia BPOM Medical Device Registration

LASSO Electrophysiology Catheter With Auto ID is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320592. 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.

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
LASSO Electrophysiology Catheter With Auto ID
Analysis ID: AKL 20501320592

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

Feb 02, 2023

Expiry Date

Aug 11, 2027

Product Type

Diagnostic Cardiology Equipment

Electrode recording catheter or electrode recording probe.

Non Electromedic Sterile

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