gudid
Primary ID: Rite Aid TRUEplus Safety Lancets
TRUEplus (UDI Rite Aid TRUEplus Safety Lancets)
Manufactured by TRIVIDIA HEALTH, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRUEplus - Primary ID Rite Aid TRUEplus Safety Lancets
Device Regulatory Overview
The TRUEplus (Model/Catalog Number: Rite Aid TRUEplus Safety Lancets) is a medical device manufactured by TRIVIDIA HEALTH, INC.. This product is indexed under FDA Product Code / Category Classification FMK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Rite Aid TRUEplus Safety Lancets
- Product Code / EMDN
- FMK
- Device Name
- Rite Aid TRUEplus Safety Lancets
- Database Sync Date
- 2026-08-09 09:00:34
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 Rite Aid TRUEplus Safety Lancets.
What classification code is assigned to this device?
This device is registered under product classification code FMK.
Similar Classification Devices (FMK)
Other Devices by TRIVIDIA HEALTH, INC.
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