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SABER™ 0.35 Percutaneous Transluminal Angioplasty (PTA) Dilation Catheter - Indonesia BPOM Medical Device Registration

SABER™ 0.35 Percutaneous Transluminal Angioplasty (PTA) Dilation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505320289. The device is manufactured by NITINOL DEVICES & COMPONENTS from Costa Rica, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. WEGO MEDIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
SABER™ 0.35 Percutaneous Transluminal Angioplasty (PTA) Dilation Catheter

SABER™ 0.35 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter

Analysis ID: AKL 20505320289

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Costa Rica

Authorized Representative

PT. WEGO MEDIKA INDONESIA

AR Address

Jl. Tanah Abang II No.67 Kel. Petojo Selatan, Kec. Gambir, Jakarta Pusat

Registration Date

Oct 22, 2023

Expiry Date

May 01, 2028

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

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