LMA ProSeal - Indonesia BPOM Medical Device Registration
LMA ProSeal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420097. The device is manufactured by PARKER HANNIFIN CSS MERRILLVILLE from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TELEFLEX MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PARKER HANNIFIN CSS MERRILLVILLECountry of Origin
United States
Authorized Representative
TELEFLEX MEDICAL INDONESIAAR Address
Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1
Registration Date
Feb 13, 2024
Expiry Date
Nov 14, 2028
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
Non Electromedic Non Sterile
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