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ARROW AC3 OPTIMUS Intra-Aortic Balloon Pump (IABP) System - Indonesia BPOM Medical Device Registration

ARROW AC3 OPTIMUS Intra-Aortic Balloon Pump (IABP) System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503420041. The device is manufactured by ARROW INTERNATIONAL LLC from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TELEFLEX MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
ARROW AC3 OPTIMUS Intra-Aortic Balloon Pump (IABP) System
Analysis ID: AKL 30503420041

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. TELEFLEX MEDICAL INDONESIA

AR Address

Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1

Registration Date

Mar 14, 2024

Expiry Date

Nov 14, 2028

Product Type

Prosthetic Cardiology Equipment

Intra-aortic balloon and control system

Non Radiation Electromedics

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