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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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BPOM Registered
Risk Class Kelas Resiko : B
TECHNOCLONE Coagulation Reference
Analysis ID: AKL 20205120162

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Austria

Authorized Representative

PT. BRIDGE TWO

AR 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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