gudid
Primary ID: VI400-911
Synermed (UDI VI400-911)
Manufactured by INFRARED LABORATORY SYSTEMS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Synermed - Primary ID VI400-911
Device Regulatory Overview
The Synermed (Model/Catalog Number: VI400-911) is a medical device manufactured by INFRARED LABORATORY SYSTEMS LLC. This product is indexed under FDA Product Code / Category Classification JFJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VI400-911
- Product Code / EMDN
- JFJ
- Device Name
- Amylase Reagent 8 X 50 mL
- Database Sync Date
- 2026-08-09 09:57:31
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 Synermed?
The registered manufacturer of record for Synermed is INFRARED LABORATORY SYSTEMS LLC.
What is the Primary UDI-DI identifier for Synermed?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VI400-911.
What classification code is assigned to this device?
This device is registered under product classification code JFJ.
Similar Classification Devices (JFJ)
Other Devices by INFRARED LABORATORY SYSTEMS LLC
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