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TECHLAB C. DIFF QUIK CHEK COMPLETE - Indonesia BPOM Medical Device Registration

TECHLAB C. DIFF QUIK CHEK COMPLETE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220453. The device is manufactured by TECHLAB INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCIENCEWERKE.

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Risk Class Kelas Resiko : B
TECHLAB C. DIFF QUIK CHEK COMPLETE
Analysis ID: AKL 20303220453

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TECHLAB INC

Country of Origin

United States

Authorized Representative

PT. SCIENCEWERKE

AR Address

Jl.Palmerah Barat No.25

Registration Date

Jul 29, 2024

Expiry Date

May 08, 2027

Product Type

Serological Reagents

Clostridium difficile toxin gene amplification assay

Invitro Diagnostics

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