eudamed_udi
Primary ID: 05060259070013
Transwab (UDI 05060259070013)
Manufactured by Medical Wire & Equipment Co Bath (Ltd)
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transwab - Primary ID 05060259070013
Device Regulatory Overview
The Transwab (Model/Catalog Number: MW169P) is a medical device manufactured by Medical Wire & Equipment Co Bath (Ltd). This product is indexed under FDA Product Code / Category Classification A1102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MW169P
- Product Code / EMDN
- A1102
- Device Name
- Transwab
- Database Sync Date
- 2026-08-09 16:45:05
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Transwab?
The registered manufacturer of record for Transwab is Medical Wire & Equipment Co Bath (Ltd).
What is the Primary UDI-DI identifier for Transwab?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060259070013.
What classification code is assigned to this device?
This device is registered under product classification code A1102.
Similar Classification Devices (A1102)
Other Devices by Medical Wire & Equipment Co Bath (Ltd)
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