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SURFLO Flash IV Catheter - Indonesia BPOM Medical Device Registration

SURFLO Flash IV Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902701894. The device is manufactured by KOFU FACTORY OF TERUMO CORPORATION JAPAN from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
SURFLO Flash IV Catheter
Analysis ID: AKL 20902701894

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

Feb 25, 2021

Expiry Date

Oct 16, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set.

Non Electromedic Sterile

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