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MAHURKAR Acute Dual Lumen Catheters and Kits - Indonesia BPOM Medical Device Registration

MAHURKAR Acute Dual Lumen Catheters and Kits is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805020918. The device is manufactured by COVIDIEN MANUFACTURING SOLUTIONS, S.A from Costa Rica, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
MAHURKAR Acute Dual Lumen Catheters and Kits
Analysis ID: AKL 20805020918

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Costa Rica

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Mar 09, 2020

Expiry Date

Apr 11, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Blood access device and accessories.

Non Electromedic Sterile

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