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HUMATEX Febrile Antigens Salmonella Typhi H - Indonesia BPOM Medical Device Registration

HUMATEX Febrile Antigens Salmonella Typhi H is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303802730. The device is manufactured by HUMAN SOCIETY FOR BIOCHEMISTRY AND DIAGNOSTICS from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SALI POLAPA TOGETHER.

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BPOM Registered
Risk Class Kelas Resiko : B
HUMATEX Febrile Antigens Salmonella Typhi H
Analysis ID: AKL 20303802730

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

SALI POLAPA TOGETHER

AR Address

Puri Sentra Niaga Blok B 33-34 Jl. Raya Kalimalang 13620

Registration Date

Feb 06, 2023

Expiry Date

Nov 08, 2027

Product Type

Serological Reagents

Salmonella spp. serological reagents.

Invitro Diagnostics

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DJ Fang

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