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TECO Factor IX Deficient Plasma - Indonesia BPOM Medical Device Registration

TECO Factor IX Deficient Plasma is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207802698. The device is manufactured by TECO MEDICAL INSTRUMENTS PRODUCTION + TRADING GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FAITHFUL MEDICAL GRACE.

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BPOM Registered
Risk Class Kelas Resiko : B
TECO Factor IX Deficient Plasma
Analysis ID: AKL 20207802698

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

Mar 10, 2023

Expiry Date

Oct 10, 2027

Product Type

Haematology Package and Kit

Factor deficiency test.

Invitro Diagnostics

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