gudid
Primary ID: FB50
Biowy Freezing Bag (UDI FB50)
Manufactured by Biowy Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Biowy Freezing Bag - Primary ID FB50
Device Regulatory Overview
The Biowy Freezing Bag (Model/Catalog Number: FB50) is a medical device manufactured by Biowy Corporation. This product is indexed under FDA Product Code / Category Classification LPZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FB50
- Product Code / EMDN
- LPZ
- Device Name
- Biowy Freezing Bag FB50, Max Volume: 50 mL
- Database Sync Date
- 2026-08-09 09:49:35
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 Biowy Freezing Bag?
The registered manufacturer of record for Biowy Freezing Bag is Biowy Corporation.
What is the Primary UDI-DI identifier for Biowy Freezing Bag?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FB50.
What classification code is assigned to this device?
This device is registered under product classification code LPZ.
Similar Classification Devices (LPZ)
Other Devices by Biowy Corporation
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