Ceveron m2 - Indonesia BPOM Medical Device Registration
Ceveron m2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205320434. The device is manufactured by TECO MEDICAL INSTRUMENTS, PRODUCTION + TRADING GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Germany
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Aug 11, 2023
Expiry Date
May 27, 2025
Product Type
Automatic and Semi-Automatic Hematology Equipment
Coagulation instrument.
Invitro Diagnostics
TECHNOCLONE AK-Calibrant
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
TECHNOCLONE Coagulation Reference
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS LTD.,
TECHNOCLONE Coagulation Control A
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS LTD.
TC Thrombin Reagent
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
ACTI-LANCE Lite Safety Lancet 28G
HTL-STREFA S.A.
TECHNOCLONE Fibrinogen Reagent Kit
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
TC Coagulation Control AK
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS LTD.
TECHNOCHROM ATIII Kit
TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH
EPIX Laparoscopic Grasper
APPLIED MEDICAL RESOURCES CORPORATION
MEDISAFE Solo, safety lancets
HTL-STREFA S.A.