BD Venflon ™ Pro IV Cannula with BD Instaflash ™ Needle Technology - Indonesia BPOM Medical Device Registration
BD Venflon ™ Pro IV Cannula with BD Instaflash ™ Needle Technology is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902421132. The device is manufactured by BECTON DICKINSON INDIA PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BECTON DICKINSON 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BECTON DICKINSON INDIA PVT. LTD.Country of Origin
India
Authorized Representative
BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Oct 07, 2024
Expiry Date
May 22, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter.
Non Electromedic Sterile
ALARIS ™ Product. SmartSite ™ Needle-free System. TRANSFUSION/BOOD SET. VENTED. 200 µm FILTER.
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