Pure Global

KingFisher DUO PRIME - Indonesia BPOM Medical Device Registration

KingFisher DUO PRIME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420011. The device is manufactured by LIFE TECHNOLOGIES HOLDING PTE. LTD. from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
KingFisher DUO PRIME
Analysis ID: AKL 20304420011

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Singapore

Authorized Representative

PT. ELO KARSA UTAMA

AR Address

Jl. Raya Kebayoran Lama No. 34E

Registration Date

Jan 19, 2024

Expiry Date

Jun 30, 2025

Product Type

Immunology Laboratory Equipment and Reagents

RNA Preanalytical Systems.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from LIFE TECHNOLOGIES HOLDING PTE. LTD.
Products from the same manufacturer (2 products)