gudid
Primary ID: Trial Pack
Calplus (UDI Trial Pack)
Manufactured by PREVEST DENPRO LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Calplus - Primary ID Trial Pack
Device Regulatory Overview
The Calplus (Model/Catalog Number: Trial Pack) is a medical device manufactured by PREVEST DENPRO LIMITED. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Trial Pack
- Product Code / EMDN
- KIF
- Device Name
- Database Sync Date
- 2026-08-09 09:01:11
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 Calplus?
The registered manufacturer of record for Calplus is PREVEST DENPRO LIMITED.
What is the Primary UDI-DI identifier for Calplus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Trial Pack.
What classification code is assigned to this device?
This device is registered under product classification code KIF.
Similar Classification Devices (KIF)
Other Devices by PREVEST DENPRO LIMITED
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