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STANDARD F Dengue IgM/IgG FIA and Accessories - Indonesia BPOM Medical Device Registration

STANDARD F Dengue IgM/IgG FIA and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303816142. The device is manufactured by SD BIOSENSOR. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. STANDARD BIOSENSOR INDONESIA.

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Risk Class Kelas Resiko : C
STANDARD F Dengue IgM/IgG FIA and Accessories
Analysis ID: AKL 20303816142

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SD BIOSENSOR.

Country of Origin

Korea

Authorized Representative

PT. STANDARD BIOSENSOR INDONESIA

AR Address

L'AVENUE BUILDING UNIT C, LT. 21, JL. RAYA PASAR MINGGU KAV. 16

Registration Date

Sep 27, 2024

Expiry Date

Jan 18, 2029

Product Type

Serological Reagents

Dengue virus serological reagents

Invitro Diagnostics

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