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ACROSS LISS - Indonesia BPOM Medical Device Registration

ACROSS LISS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204513203. The device is manufactured by DIAPRO TIBBI URUNLER SAN. VE TIC. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MITRA BAHAGIA CITRA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : A
ACROSS LISS
Analysis ID: AKL 10204513203

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Turkey

Authorized Representative

MITRA BAHAGIA CITRA MEDIKA

AR Address

Jl. Raya Kalirungkut 27 Blok C-63

Registration Date

Jan 11, 2024

Expiry Date

Dec 31, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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