HUMAN HUMATEX Febrile Antigens Salmonella Typhi BO - Indonesia BPOM Medical Device Registration

HUMAN HUMATEX Febrile Antigens Salmonella Typhi BO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303803079. The device is manufactured by HUMAN Gesellschaft für Biochemica und Diagnostica mbH 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

HUMAN HUMATEX Febrile Antigens Salmonella Typhi BO

Analysis ID: AKL 20303803079

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HUMAN Gesellschaft für Biochemica und Diagnostica mbH

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

DJ Fang

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HUMAN HUMATEX Febrile Antigens Salmonella Typhi BO - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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