ID LAB FIA Analyzer - Indonesia BPOM Medical Device Registration

ID LAB FIA Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304124052. The device is manufactured by AEHEALTH LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOLAB ARTHA MEDIKA.

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BPOM Registered

Risk Class Kelas Resiko : B

ID LAB FIA Analyzer

Analysis ID: AKL 20304124052

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AEHEALTH LIMITED

Country of Origin

United Kingdom

Authorized Representative

PT. INDOLAB ARTHA MEDIKA

AR Address

Komp Ruko Sunter Paradise Tahap II Blok.A4 No.43. Sunter Agung Podomoro

Registration Date

Jul 09, 2021

Expiry Date

Jul 09, 2024

Product Type

Immunology Laboratory Equipment and Reagents

Immunofluorometer equipment

Invitro Diagnostics

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ID LAB FIA Analyzer - 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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