SPROTTE® Cannula - Indonesia BPOM Medical Device Registration
SPROTTE® Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403212413. The device is manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PAJUNK GMBH MEDIZINTECHNOLOGIECountry of Origin
Germany
Authorized Representative
PT. BRIDGE TWOAR Address
Petojo Melintang No. 17 Kel. Petojo Selatan, Kec. Gambir Jakarta Pusat
Registration Date
Aug 12, 2022
Expiry Date
Aug 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Anesthesia conduction needle.
Non Electromedic Sterile
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DELTACUT Biopsy
INTRALONG Kit
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PAJUNK SonoTap Cannula
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TECHNOCLONE Coagulation Control A
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TC Thrombin Reagent
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ACTI-LANCE Lite Safety Lancet 28G
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TECHNOCLONE Fibrinogen Reagent Kit
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TC Coagulation Control AK
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TECHNOCHROM ATIII Kit
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EPIX Laparoscopic Grasper
APPLIED MEDICAL RESOURCES CORPORATION
MEDISAFE Solo, safety lancets
HTL-STREFA S.A.