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CITODIA Saliva Collection Kit - Indonesia BPOM Medical Device Registration

CITODIA Saliva Collection Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302220114. The device is manufactured by CITOTEST LABWARE MANUFACTURING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DIAGNOSIS OF INNOVASI.

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BPOM Registered
Risk Class Kelas Resiko : A
CITODIA Saliva Collection Kit
Analysis ID: AKL 10302220114

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. DIAGNOSIS OF INNOVASI

AR Address

Prodia Tower, Jl. Kramat Raya No. 150 Kel. Kenari, Kec. Senen - Jakarta Pusat 10430

Registration Date

Aug 15, 2022

Expiry Date

Jun 29, 2025

Product Type

Microbiology Equipment

Microbiological specimen collection and transport device.

Invitro Diagnostics

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