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FINETHROUGH Sterile Cardiovascular Guidewire - Indonesia BPOM Medical Device Registration

FINETHROUGH Sterile Cardiovascular Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501127785. The device is manufactured by SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD. from China, 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
FINETHROUGH Sterile Cardiovascular Guidewire
Analysis ID: AKL 20501127785

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. REKAMILENIUMINDO SELARAS

AR Address

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

Registration Date

Apr 27, 2022

Expiry Date

Oct 14, 2026

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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