gudid
Primary ID: 1925X
All American (UDI 1925X)
Manufactured by WISCONSIN ALUMINUM FOUNDRY COMPANY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for All American - Primary ID 1925X
Device Regulatory Overview
The All American (Model/Catalog Number: 1925X) is a medical device manufactured by WISCONSIN ALUMINUM FOUNDRY COMPANY, INC.. This product is indexed under FDA Product Code / Category Classification FLE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1925X
- Product Code / EMDN
- FLE
- Device Name
- Table top non-electric steam sterilizer
- Database Sync Date
- 2026-08-09 09:08:43
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 All American?
The registered manufacturer of record for All American is WISCONSIN ALUMINUM FOUNDRY COMPANY, INC..
What is the Primary UDI-DI identifier for All American?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1925X.
What classification code is assigned to this device?
This device is registered under product classification code FLE.
Similar Classification Devices (FLE)
Other Devices by WISCONSIN ALUMINUM FOUNDRY COMPANY, INC.
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