Pure Global

IDKmonitor Infliximab total ADA ELISA - Indonesia BPOM Medical Device Registration

IDKmonitor Infliximab total ADA ELISA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305917140. The device is manufactured by IMMUNDIAGNOSTIK AG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INTI MAKMUR MEDITAMA.

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
IDKmonitor Infliximab total ADA ELISA
Analysis ID: AKL 20305917140

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

IMMUNDIAGNOSTIK AG

Country of Origin

Germany

Authorized Representative

INTI MAKMUR MEDITAMA

AR Address

JL. SULTAN ISKANDAR MUDA, GANDARIA 8 OFFICE TOWER LANTAI 16 UNIT F, KEBAYORAN LAMA JAKARTA SELATAN

Registration Date

Nov 01, 2019

Expiry Date

Feb 18, 2024

Product Type

Immunological Test System

Rheumatoid factor immunological test system.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing