Pure Global

FRESENIUS KABI Extension 3-fold, K-NECT, BCV, LLM, DEHP-free, Latex-free - Indonesia BPOM Medical Device Registration

FRESENIUS KABI Extension 3-fold, K-NECT, BCV, LLM, DEHP-free, Latex-free is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902610513. The device is manufactured by CLINICO MEDICAL SP.Z.O.O. from Poland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS KABI 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
FRESENIUS KABI Extension 3-fold, K-NECT, BCV, LLM, DEHP-free, Latex-free
Analysis ID: AKL 20902610513

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870

Registration Date

Apr 22, 2020

Expiry Date

Jul 26, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing