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EMPIRA™ RX PTCA Dilatation Catheter - Indonesia BPOM Medical Device Registration

EMPIRA™ RX PTCA Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505810480. The device is manufactured by CREGANNA MEDICAL from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CEKINDO BISNIS GRUP.

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BPOM Registered
Risk Class Kelas Resiko : C
EMPIRA™ RX PTCA Dilatation Catheter
Analysis ID: AKL 20505810480

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

CREGANNA MEDICAL

Country of Origin

Singapore

Authorized Representative

PT. CEKINDO BISNIS GRUP

AR Address

Jln. Raya Meruya Ilir Raya Kav 88. Business Park Kebon Jeruk Blok H1-H2 RT 008 RW 007.

Registration Date

Nov 16, 2021

Expiry Date

Sep 08, 2025

Product Type

Therapeutic Cardiology Equipment

Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Non Electromedic Sterile

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