Pure Global

IMMUNEMED Leptospira Rapid - Indonesia BPOM Medical Device Registration

IMMUNEMED Leptospira Rapid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303913499. The device is manufactured by IMMUNEMED INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOCORE PERKASA.

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 : B
IMMUNEMED Leptospira Rapid
Analysis ID: AKL 20303913499

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

IMMUNEMED INC.

Country of Origin

Korea

Authorized Representative

INDOCORE PERKASA

AR Address

Komplek Graha Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006 Kelurahan : Jati Kecamatan : Pulo Gadung Jakarta Timur 13220

Registration Date

May 29, 2019

Expiry Date

Mar 31, 2024

Product Type

Serological Reagents

Leptospira spp. serological reagents.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from IMMUNEMED INC.
Products from the same manufacturer (2 products)