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CUDA Surgical Xenon Light Source - Indonesia BPOM Medical Device Registration

CUDA Surgical Xenon Light Source is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420009. The device is manufactured by SUNOPTIC TECHNOLOGIES from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LUMARY BIRUMAS.

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.

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BPOM Registered
Risk Class Kelas Resiko : B
CUDA Surgical Xenon Light Source
Analysis ID: AKL 20801420009

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. LUMARY BIRUMAS

AR Address

Gd. Menara Palma Lt. 12 Jl. H.R. Rasuna Said Blok X-2, Kav.6 Jakarta 12950

Registration Date

Jan 04, 2024

Expiry Date

Jun 26, 2028

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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