Pure Global

AGAPPE Mispa-i3 C3 - Indonesia BPOM Medical Device Registration

AGAPPE Mispa-i3 C3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305520080. The device is manufactured by AGAPPE DIAGNOSTICS LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.

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
AGAPPE Mispa-i3 C3
Analysis ID: AKL 20305520080

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. MULTIMEDILAB KARYAMANDIRI

AR Address

GP PLAZA LANTAI 3 UNIT 6 JALAN GELORA II NOMOR 01

Registration Date

Feb 10, 2025

Expiry Date

Feb 07, 2027

Product Type

Immunological Test System

Complement components immunological test system.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing