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PRELUDE + NEEDLE SHEATH INTRODUCER - Indonesia BPOM Medical Device Registration

PRELUDE + NEEDLE SHEATH INTRODUCER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320818. 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. REKAMILENIUMINDO SELARAS.

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BPOM Registered
Risk Class Kelas Resiko : C
PRELUDE + NEEDLE SHEATH INTRODUCER
Analysis ID: AKL 20501320818

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. REKAMILENIUMINDO SELARAS

AR Address

Jl. Tomang Raya No. 51B RT 01 RW 05, Kelurahan Tomang

Registration Date

Jun 11, 2023

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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