PARKER Laryngeal Mask Device - Indonesia BPOM Medical Device Registration
PARKER Laryngeal Mask Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403814757. The device is manufactured by WELL LEAD MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WELL LEAD MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Jan 24, 2025
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
Non Electromedic Sterile
VIDA Feeding Tube
PARKER Flex-Tip PFRU (Reinforced Uncuffed)
PARKER FLEX-TIP® PFOC (Preformed Oral Cuffed)
PARKER FLEX-TIP® PFNU (Preformed Nasal Uncuffed)
PARKER ThinCuff PTCY (Murphy-type tracheal tube)
PARKER FLEX-TIP® PFNC (Preformed Nasal Cuffed)
PARKER THINCUFF PTCL (Magill-type tracheal tube)
PARKER FLEX-TIP® PFOU (Preformed Oral Uncuffed)
PARKER Flex-Tip PFRC (Reinforced Cuffed)
PARKER FLEX-TIP PFUO (Uncuffed)
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PARKER ThinCuff PTCY (Murphy-type tracheal tube)
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PARKER THINCUFF PTCL (Magill-type tracheal tube)
WELL LEAD MEDICAL CO., LTD.
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