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TECHNOPLASTIN HIS f. Ceveron - Indonesia BPOM Medical Device Registration

TECHNOPLASTIN HIS f. Ceveron is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207121995. The device is manufactured by TECHNOCLONE MANUFACTURING OF DIAGNOSTICS AND PHARMACEUTICALS GMBH from Austria, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BRIDGE TWO.

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BPOM Registered
Risk Class Kelas Resiko : C
TECHNOPLASTIN HIS f. Ceveron
Analysis ID: AKL 20207121995

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Austria

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Jan 02, 2025

Expiry Date

Dec 31, 2027

Product Type

Haematology Package and Kit

Prothrombin time test.

Invitro Diagnostics

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