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BIOPANDA NT-proBNP Rapid Test - Indonesia BPOM Medical Device Registration

BIOPANDA NT-proBNP Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421863. The device is manufactured by BIOPANDA REAGENTS LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.

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
BIOPANDA NT-proBNP Rapid Test
Analysis ID: AKL 20101421863

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. ANDAMAN MEDICAL INDONESIA

AR Address

Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma

Registration Date

Sep 24, 2024

Expiry Date

Apr 25, 2027

Product Type

Clinical Chemistry Test System

B-type natriuretic peptide test system (kit & cair)

Invitro Diagnostics

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