TECHNOCLONE Coagulation Reference - Indonesia BPOM Medical Device Registration
TECHNOCLONE Coagulation Reference is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205120162. The device is manufactured by TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS LTD., from Austria, 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
Country of Origin
Austria
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Feb 10, 2025
Expiry Date
Dec 31, 2027
Product Type
Automatic and Semi-Automatic Hematology Equipment
Multipurpose system for in vitro coagulation studies
Invitro Diagnostics
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