gudid
Primary ID: 25040
PouchPro (UDI 25040)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PouchPro - Primary ID 25040
Device Regulatory Overview
The PouchPro (Model/Catalog Number: 25040) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification IYE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 25040
- Product Code / EMDN
- IYE
- Device Name
- Sample, SecureFoam - Pouch-Pro, Medium
- Database Sync Date
- 2026-08-09 09:04:11
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 PouchPro?
The registered manufacturer of record for PouchPro is Bionix, LLC.
What is the Primary UDI-DI identifier for PouchPro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 25040.
What classification code is assigned to this device?
This device is registered under product classification code IYE.
Similar Classification Devices (IYE)
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