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DUMOLABS Salmonella Paratyphi CO - Indonesia BPOM Medical Device Registration

DUMOLABS Salmonella Paratyphi CO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303122684. The device is manufactured by DIALAB G.M.B.H from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DUMO DIAGNOSTICS INDONESIA.

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Risk Class Kelas Resiko : B
DUMOLABS Salmonella Paratyphi CO
Analysis ID: AKL 20303122684

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DIALAB G.M.B.H

Country of Origin

Austria

Authorized Representative

PT. DUMO DIAGNOSTICS INDONESIA

AR Address

JL. KALIBATA SELATAN II NO 2 RT 002/04 KEL. KALIBATA, KEC. PANCORAN, JAKARTA SELATAN

Registration Date

May 06, 2021

Expiry Date

May 06, 2024

Product Type

Serological Reagents

Salmonella spp. serological reagents.

Invitro Diagnostics

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