GUDIDData
gudid Primary ID: Plain

Transwab (UDI Plain)

Manufactured by MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transwab - Primary ID Plain

Device Regulatory Overview

The Transwab (Model/Catalog Number: Plain) is a medical device manufactured by MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED. This product is indexed under FDA Product Code / Category Classification LIO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Plain
Product Code / EMDN
LIO
Device Name
Transwab ENT Amies Medium
Database Sync Date
2026-08-09 09:57:34

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Transwab?

The registered manufacturer of record for Transwab is MEDICAL WIRE & EQUIPMENT CO.(BATH)LIMITED.

What is the Primary UDI-DI identifier for Transwab?

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

What classification code is assigned to this device?

This device is registered under product classification code LIO.

Programmatic Export

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