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LANSIONBIO PCT Test Kit (Dry Fluorescence Immunoassay) - Indonesia BPOM Medical Device Registration

LANSIONBIO PCT Test Kit (Dry Fluorescence Immunoassay) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321383. The device is manufactured by LANSION BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIORITA DIAN SARANA.

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 : B
LANSIONBIO PCT Test Kit (Dry Fluorescence Immunoassay)
Analysis ID: AKL 20303321383

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PRIORITA DIAN SARANA

AR Address

Jl. RSI. Faisal Raya No. 06

Registration Date

Sep 02, 2023

Expiry Date

May 08, 2028

Product Type

Serological Reagents

Procalcitonin test system

Invitro Diagnostics

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