AMBU AuraGain Single Use Laryngeal Mask - Indonesia BPOM Medical Device Registration
AMBU AuraGain Single Use Laryngeal Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420019. The device is manufactured by AMBU., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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
PT. AMI MEDIKA INDONESIAAR Address
The Savoy B1-30, Jakarta Garden City Boulevard
Registration Date
Jan 11, 2024
Expiry Date
Aug 31, 2028
Product Type
Therapeutic Anesthesia Equipment
Tracheostomy tube and tube cuff.
Non Electromedic Sterile
AMBU Oval Plus Silicone Resuscitator
AMBU., LTD.
AMBU SPUR II Resuscitator
AMBU., LTD.
AMBU Mark lV Resuscitator
AMBU., LTD.
AMBU Aura-I Single Use Laryngeal Mask
AMBU., LTD.
AMBU AuraOnce
AMBU, LTD.
Ambu aScopeโข4 Broncho
AMBU A/S
AMBU aView โข 2 Advance
BRITEMED TECHNOLOGY INC
KING Anesthesia Breathing Circuit
KING SYSTEMS
Ambu aScopeโข4 RhinoLaryngo
AMBU A/S
AMBUยฎ King Mask
AMBU A/S

