LMA Flexible Single Use - Indonesia BPOM Medical Device Registration
LMA Flexible Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420676. The device is manufactured by PLAXTRON INDUSTRIAL (M) SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TELEFLEX MEDICAL 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
PLAXTRON INDUSTRIAL (M) SDN. BHD.Country of Origin
Malaysia
Authorized Representative
PT. TELEFLEX MEDICAL INDONESIAAR Address
Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1
Registration Date
Oct 09, 2024
Expiry Date
Nov 14, 2028
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway.
Non Electromedic Sterile
ARROW Arrowg+ard Blue Advance Peripheral Inserted Central Catheter (PICC)
ARROW INTERNACIONAL DE CHIHUAHUA S.A. DE C.V.
LMA Supreme
THE LARYNGEAL MASK COMPANY (MALAYSIA) SDN. BHD.
ARROW Two-Lumen CVC
ARROW INTERNACIONAL DE CHIHUAHUA S.A. DE C.V.
LMA Gastro Cuff Pilot
THE LARYNGEAL MASK COMPANY (MALAYSIA) SDN. BHD.
ARROW Three Lumen Central Venous Catheter (CVC)
ARROW INTERNATIONAL CR, A.S.
LMA Protector Cuff Pilot
THE LARYNGEAL MASK COMPANY (MALAYSIA) SDN. BHD.
RUSCH EZ-Blocker Kit
ARROW INTERNATIONAL CR, A.S.
ARROW One-Lumen CVC
ARROW INTERNACIONAL DE CHIHUAHUA S.A. DE C.V.
ARROW Thermodilution Catheter
ARROW INTERNATIONAL LLC.
RUSCH Curved Reinforced Endotracheal Tube
TELEFLEX MEDICAL SDN. BHD.