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EM-Embolectomy Catheter ( Single Lumen ) - Indonesia BPOM Medical Device Registration

EM-Embolectomy Catheter ( Single Lumen ) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505716221. The device is manufactured by Z.T.S. HAGMED ZAJฤ„C I TOMASZEWSKI SP. J. from Poland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PELITA BIOMEDICAL.

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Risk Class Kelas Resiko : C
EM-Embolectomy Catheter ( Single Lumen )
Analysis ID: AKL 20505716221

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. PELITA BIOMEDICAL

AR Address

Gedung Autobridal Lantai4 Jl. KH Abdullah Syafei No.30 Kel. Asem Baris Kec. Tebet Jakarta Selatan

Registration Date

Dec 15, 2020

Expiry Date

Jul 01, 2025

Product Type

Therapeutic Cardiology Equipment

Embolectomy catheter.

Non Electromedic Sterile

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