Pure Global

ENFit GraviSet Bag - Indonesia BPOM Medical Device Registration

ENFit GraviSet Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902020626. The device is manufactured by FRESENIUS KABI (NANCHANG) CO., LTD from China, 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
ENFit GraviSet Bag
Analysis ID: AKL 20902020626

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

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

Feb 21, 2020

Expiry Date

May 16, 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
Other Products from FRESENIUS KABI (NANCHANG) CO., LTD
Products from the same manufacturer (2 products)