gudid
Primary ID: 1501251
Duploject Easy Prep (UDI 1501251)
Manufactured by BAXTER INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Duploject Easy Prep - Primary ID 1501251
Device Regulatory Overview
The Duploject Easy Prep (Model/Catalog Number: 1501251) is a medical device manufactured by BAXTER INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification FMF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1501251
- Product Code / EMDN
- FMF
- Device Name
- Fibrin Sealant Preparation and Application System for the preparation and application of Tisseel Two-component Fibrin Sealant (4 mL Kit)
- 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 Duploject Easy Prep?
The registered manufacturer of record for Duploject Easy Prep is BAXTER INTERNATIONAL INC..
What is the Primary UDI-DI identifier for Duploject Easy Prep?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1501251.
What classification code is assigned to this device?
This device is registered under product classification code FMF.
Similar Classification Devices (FMF)
Other Devices by BAXTER INTERNATIONAL INC.
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