gudid
Primary ID: 900-MFL
Montage Flowable Dispenser (UDI 900-MFL)
Manufactured by ABYRX, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Montage Flowable Dispenser - Primary ID 900-MFL
Device Regulatory Overview
The Montage Flowable Dispenser (Model/Catalog Number: 900-MFL) is a medical device manufactured by ABYRX, INC.. This product is indexed under FDA Product Code / Category Classification MTJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 900-MFL
- Product Code / EMDN
- MTJ
- Device Name
- Database Sync Date
- 2026-08-09 09:49:39
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 Montage Flowable Dispenser?
The registered manufacturer of record for Montage Flowable Dispenser is ABYRX, INC..
What is the Primary UDI-DI identifier for Montage Flowable Dispenser?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 900-MFL.
What classification code is assigned to this device?
This device is registered under product classification code MTJ.
Similar Classification Devices (MTJ)
Other Devices by ABYRX, INC.
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