eudamed_udi Primary ID: 13661657054231

Mucus collector (UDI 13661657054231)

Manufactured by Cair LGL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Mucus collector (Model/Catalog Number: AM040-0) is a medical device manufactured by Cair LGL. This product is indexed under FDA Product Code / Category Classification R05010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AM040-0
Product Code / EMDN: R05010301
Device Name: Class Is - Sterile devices allowing removing from patient
Database Sync Date: 2026-08-09 16:29:47

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 Mucus collector?

The registered manufacturer of record for Mucus collector is Cair LGL.

What is the Primary UDI-DI identifier for Mucus collector?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13661657054231.

What classification code is assigned to this device?

This device is registered under product classification code R05010301.

Similar Classification Devices (R05010301)

Other Devices by Cair LGL

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