Pure Global

OPTIMA Neo Standard Otoscope 2.5v (Fiber) Xenon - Indonesia BPOM Medical Device Registration

OPTIMA Neo Standard Otoscope 2.5v (Fiber) Xenon is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703126663. The device is manufactured by TIMESCO HEALTHCARE LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MITRA PHARMA 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 : A
OPTIMA Neo Standard Otoscope 2.5v (Fiber) Xenon

OPTIMA Neo Standard Otoscope 2.5v (Fibre) Xenon

Analysis ID: AKL 10703126663

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United Kingdom

Authorized Representative

PT. MITRA PHARMA INDONESIA

AR Address

Jl. Bukti Gading Villa Jl. Kuta Elok No. 06 Kelapa Gading Jakarta Timur

Registration Date

Nov 07, 2021

Expiry Date

Sep 12, 2026

Product Type

Ear, Nose and Throat Surgical Equipment

Otoscope.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing