Pure Global

TARGET-I Port CVP Port - Indonesia BPOM Medical Device Registration

TARGET-I Port CVP Port is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902125795. The device is manufactured by MEDITECH DEVICES PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. AGRAPANA MULIA MEDIKA.

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
TARGET-I Port CVP Port
Analysis ID: AKL 20902125795

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. AGRAPANA MULIA MEDIKA

AR Address

ITC Cempaka Mas Mega Grosir Lantai 8 No 8A Jl. Letjend Suprapto Kav.1

Registration Date

Mar 18, 2024

Expiry Date

Mar 17, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Subcutaneous, implanted, intravascular infusion port and catheter.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing