XPRESFIX Transparent Plaster (IV) - Indonesia BPOM Medical Device Registration
XPRESFIX Transparent Plaster (IV) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902220014. The device is manufactured by ZHEJIANG AOKI MEDICAL DRESSING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GIDION JAYA.
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XPRESFIX Plester Transparan (IV)
Risk Classification
Product Class
Kelas : 1
Manufacturer
ZHEJIANG AOKI MEDICAL DRESSING CO., LTD.Country of Origin
China
Authorized Representative
PT. GIDION JAYAAR Address
JL SULTAN HASANUDIN RT 005 / RW 05, AMBON 97128, MALUKU
Registration Date
Nov 28, 2024
Expiry Date
Nov 27, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter securement device.
Non Electromedic Sterile
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XPRESFIX Transparent Plaster
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XPRESFIX Transparent Plaster + Pad
ZHEJIANG AOKI MEDICAL DRESSING CO., LTD.
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GIDCARE Single Use Hypodermic Needle
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GIDCARE Single Use Syringe with Hypodermic Needle
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GIDCARE Disposable Blood Tranfusion Set
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XPRESFIX Medical Tape Roll
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