TRUEplus (UDI TRUEplus 3-Bevel Pen Needle 31G/5mm - 100ct box)
Manufactured by TRIVIDIA HEALTH, INC.
Device Regulatory Overview
The TRUEplus (Model/Catalog Number: TRUEplus 3-Bevel Pen Needle 31G/5mm - 100ct box) is a medical device manufactured by TRIVIDIA HEALTH, INC.. This product is indexed under FDA Product Code / Category Classification FMI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TRUEplus 3-Bevel Pen Needle 31G/5mm - 100ct box
- Product Code / EMDN
- FMI
- Device Name
- TRUEplus 3-Bevel Pen Needle 31G/5mm - 100ct box
- Database Sync Date
- 2026-08-09 09:00:33
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 TRUEplus?
The registered manufacturer of record for TRUEplus is TRIVIDIA HEALTH, INC..
What is the Primary UDI-DI identifier for TRUEplus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TRUEplus 3-Bevel Pen Needle 31G/5mm - 100ct box.
What classification code is assigned to this device?
This device is registered under product classification code FMI.
Similar Classification Devices (FMI)
Other Devices by TRIVIDIA HEALTH, INC.
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