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LIAISON H. Pylori IgG Control Set - Indonesia BPOM Medical Device Registration

LIAISON H. Pylori IgG Control Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220535. The device is manufactured by DIASORIN INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
LIAISON H. Pylori IgG Control Set
Analysis ID: AKL 20303220535

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DIASORIN INC

Country of Origin

United States

Authorized Representative

PT. BIOMEDIKAL SCIENTIFIC INDONESIA

AR Address

18 Office Park 22nd F1 Suite E, F &G, Jalan TB SIMATUPANG 18

Registration Date

Aug 23, 2022

Expiry Date

May 20, 2026

Product Type

Serological Reagents

Campylobacter fetus serological reagents.

Invitro Diagnostics

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