gudid Primary ID: L1(D19)

Breathing Tube (L1) (UDI L1(D19))

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Breathing Tube (L1) (Model/Catalog Number: L1(D19)) is a medical device manufactured by BMC Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification BZO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: L1(D19)
Product Code / EMDN: BZO
Device Name: Breathing Tube (L1)
Database Sync Date: 2026-08-09 09:05:26

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 Breathing Tube (L1)?

The registered manufacturer of record for Breathing Tube (L1) is BMC Medical Co., Ltd..

What is the Primary UDI-DI identifier for Breathing Tube (L1)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L1(D19).

What classification code is assigned to this device?

This device is registered under product classification code BZO.

Similar Classification Devices (BZO)

Other Devices by BMC Medical Co., Ltd.

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