gudid Primary ID: MLB+350

Sun Nuclear MICRO+ (UDI MLB+350)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Sun Nuclear MICRO+ (Model/Catalog Number: MLB+350) is a medical device manufactured by SUN NUCLEAR CORP.. This product is indexed under FDA Product Code / Category Classification IWE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MLB+350
Product Code / EMDN: IWE
Device Name: The MICRO+ MLB+350 Laser is used for aligning patients to medical diagnostic imaging and radiation therapy equipment which utilizes ionizing radiation. This product is used in medical clinic or hospital settings by trained medical staff. The lasers are not designed to be used around flammable anesthetics, which might present a risk of explosion or fire. The lasers are not intended to be used in a sterile or corrosive environment. No other uses are intended or implied.
Database Sync Date: 2026-08-09 09:43:55

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Sun Nuclear MICRO+?

The registered manufacturer of record for Sun Nuclear MICRO+ is SUN NUCLEAR CORP..

What is the Primary UDI-DI identifier for Sun Nuclear MICRO+?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MLB+350.

What classification code is assigned to this device?

This device is registered under product classification code IWE.

Similar Classification Devices (IWE)

Other Devices by SUN NUCLEAR CORP.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint