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CLARIVEIN Infusion Catheter - Indonesia BPOM Medical Device Registration

CLARIVEIN Infusion Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501027829. The device is manufactured by MERIT MEDICAL SYSTEMS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NUGRA KARSERA.

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BPOM Registered
Risk Class Kelas Resiko : C
CLARIVEIN Infusion Catheter
Analysis ID: AKL 20501027829

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Sep 25, 2021

Expiry Date

Dec 31, 2023

Product Type

Diagnostic Cardiology Equipment

Continuous flush catheter.

Non Radiation Electromedics

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