Pure Global

VIDA Infusion Set Adult - Indonesia BPOM Medical Device Registration

VIDA Infusion Set Adult is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420525. The device is manufactured by SHANGHAI MEDIC INDUSTRY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DANVI MEDILAB PERKASA.

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
VIDA Infusion Set Adult
Analysis ID: AKL 20902420525

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DANVI MEDILAB PERKASA

AR Address

Jl. Kapten Muslim Komp. Mega Com Center Blok G No. 1-2 Kel. Dwikora Kec. Medan Helvetia

Registration Date

May 31, 2024

Expiry Date

May 30, 2027

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
Similar Products (1)
Other products with the same name