eudamed_udi Primary ID: 13661657058673

Extension sets (UDI 13661657058673)

Manufactured by Cair LGL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Extension sets (Model/Catalog Number: PB3120MF-0) is a medical device manufactured by Cair LGL. This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PB3120MF-0
Product Code / EMDN: A03020101
Device Name: Class IIa - Sterile devices for infusion
Database Sync Date: 2026-08-09 16:29:09

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 Extension sets?

The registered manufacturer of record for Extension sets is Cair LGL.

What is the Primary UDI-DI identifier for Extension sets?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13661657058673.

What classification code is assigned to this device?

This device is registered under product classification code A03020101.

Similar Classification Devices (A03020101)

Other Devices by Cair LGL

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