lambda 2 (UDI 08033638321768)

Manufactured by LED SpA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The lambda 2 (Model/Catalog Number: LMB002) is a medical device manufactured by LED SpA. This product is indexed under FDA Product Code / Category Classification Z120615 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: LMB002
Product Code / EMDN: Z120615
Device Name: lambda 2
Database Sync Date: 2026-08-09 16:45:04

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of lambda 2?

The registered manufacturer of record for lambda 2 is LED SpA.

What is the Primary UDI-DI identifier for lambda 2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033638321768.

What classification code is assigned to this device?

This device is registered under product classification code Z120615.

Similar Classification Devices (Z120615)

Other Devices by LED SpA

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