gudid
Primary ID: 127-W
WNL (UDI 127-W)
Manufactured by FOREMOUNT ENTERPRISE CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WNL - Primary ID 127-W
Device Regulatory Overview
The WNL (Model/Catalog Number: 127-W) is a medical device manufactured by FOREMOUNT ENTERPRISE CO., LTD.. This product is indexed under FDA Product Code / Category Classification CBP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 127-W
- Product Code / EMDN
- CBP
- Device Name
- CPR Resuscitator mask in Zip-Lok Bag w/ Glove & Wipe
- Database Sync Date
- 2026-08-09 09:15:28
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 WNL?
The registered manufacturer of record for WNL is FOREMOUNT ENTERPRISE CO., LTD..
What is the Primary UDI-DI identifier for WNL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 127-W.
What classification code is assigned to this device?
This device is registered under product classification code CBP.
Similar Classification Devices (CBP)
Other Devices by FOREMOUNT ENTERPRISE CO., LTD.
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