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FiCA – I FIA Analyzer - Indonesia BPOM Medical Device Registration

FiCA – I FIA Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420105. The device is manufactured by SURE BIO-TECH (USA) CO., LTD from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOLAB ARTHA MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
FiCA – I FIA Analyzer
Analysis ID: AKL 20304420105

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. INDOLAB ARTHA MEDIKA

AR Address

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

Registration Date

Nov 06, 2024

Expiry Date

Jan 31, 2029

Product Type

Immunology Laboratory Equipment and Reagents

Immunofluorometer equipment. (Electrically Operated)

Invitro Diagnostics

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