Pure Global

MEDITAPE UC-12S - Indonesia BPOM Medical Device Registration

MEDITAPE UC-12S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101717660. The device is manufactured by EIKEN CHEMICAL, CO, LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SYSMEX 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
MEDITAPE UC-12S
Analysis ID: AKL 20101717660

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. SYSMEX INDONESIA

AR Address

Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13

Registration Date

Jan 31, 2022

Expiry Date

Jan 28, 2026

Product Type

Clinical Chemistry Test System

Multi parameter clinical chemistry test system

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from EIKEN CHEMICAL, CO, LTD.
Products from the same manufacturer (1 products)