AMBU Mark IV Resuscitator - Indonesia BPOM Medical Device Registration
AMBU Mark IV Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420216. The device is manufactured by AMBU., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AMI MEDIKA 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
AMBU., LTD.Country of Origin
China
Authorized Representative
AMI MEDIKA INDONESIAAR Address
The Savoy B1-30, Jakarta Garden City Boulevard
Registration Date
Mar 13, 2024
Expiry Date
Aug 31, 2028
Product Type
Therapeutic Anesthesia Equipment
Manual emergency ventilator.
Non Electromedic Non Sterile

