Pure Global

SUNOPTIC Xenon Light Sources Titan X300 - Indonesia BPOM Medical Device Registration

SUNOPTIC Xenon Light Sources Titan X300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801125914. The device is manufactured by SUNOPTIC TECHNOLOGIES LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PERMATA MEDIKA PRIMA.

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
SUNOPTIC Xenon Light Sources Titan X300
Analysis ID: AKL 20801125914

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. PERMATA MEDIKA PRIMA

AR Address

JL. HOS COKROAMINOTO, PERTOKOAN CBD CILEDUG BLOK A3 NO. 30, RT.001/RW.001

Registration Date

Sep 12, 2023

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing