VIDA Endotracheal Tube With Cuff - Indonesia BPOM Medical Device Registration
VIDA Endotracheal Tube With Cuff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403520087. The device is manufactured by HANGZHOU FORMED MEDICAL DEVICES CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU FORMED MEDICAL DEVICES CO.,LTD.Country of Origin
China
Authorized Representative
DANVI MEDILAB PERKASAAR Address
Jl. Kapten Muslim Komp. Mega Com Center Blok G No. 1-2 Kel. Dwikora Kec. Medan Helvetia
Registration Date
Jan 30, 2025
Expiry Date
Jan 29, 2028
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
Non Electromedic Sterile
