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GENEPROOF Bordetella pertussis/parapertussis PCR Kit - Indonesia BPOM Medical Device Registration

GENEPROOF Bordetella pertussis/parapertussis PCR Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321464. The device is manufactured by GENEPROOF A.S. from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOSAINS MEDIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
GENEPROOF Bordetella pertussis/parapertussis PCR Kit
Analysis ID: AKL 20303321464

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GENEPROOF A.S.

Country of Origin

Czech Republic

Authorized Representative

PT. BIOSAINS MEDIKA INDONESIA

AR Address

PLAZA KARINDA BLOK B1/4, JALAN KARANG TENGAH RAYA

Registration Date

Oct 11, 2023

Expiry Date

Mar 26, 2026

Product Type

Serological Reagents

Bordetella spp. serological reagents.

Invitro Diagnostics

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DJ Fang

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