Pure Global

HEADWAY Microcatheter - Indonesia BPOM Medical Device Registration

HEADWAY Microcatheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501124324. The device is manufactured by MICROVENTION COSTA RICA S.R.L. from Costa Rica, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ADMIRAL BLESENSA IMMORTAL.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
HEADWAY Microcatheter
Analysis ID: AKL 20501124324

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Costa Rica

Authorized Representative

PT. ADMIRAL BLESENSA IMMORTAL

AR Address

Ruko Graha Handaya unit H Jl. Raya Pejuangan Kav. 12A, Kebon Jeruk, Kota Jakarta Barat, Kode Pos 11530

Registration Date

Apr 20, 2023

Expiry Date

Feb 03, 2027

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing