Pure Global

ARAGAN Plus Injection - Indonesia BPOM Medical Device Registration

ARAGAN Plus Injection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302711568. The device is manufactured by DONGKWANG PHARM CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. 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 : D
ARAGAN Plus Injection
Analysis ID: AKL 31302711568

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Korea

Authorized Representative

PT. FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73

Registration Date

Nov 28, 2023

Expiry Date

Jun 12, 2025

Product Type

Prosthetic Orthopedic Equipment

Intra articular fluid

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from DONGKWANG PHARM CO., LTD.
Products from the same manufacturer (1 products)