gudid
Primary ID: CUSBHOLTER
CardioCard Holter (UDI CUSBHOLTER)
Manufactured by NASIFF ASSOCIATES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CardioCard Holter - Primary ID CUSBHOLTER
Device Regulatory Overview
The CardioCard Holter (Model/Catalog Number: CUSBHOLTER) is a medical device manufactured by NASIFF ASSOCIATES INC. This product is indexed under FDA Product Code / Category Classification DRT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CUSBHOLTER
- Product Code / EMDN
- DRT
- Device Name
- Cardio Card Holter, Ambulatory, Mobile System.
- Database Sync Date
- 2026-08-09 09:03:51
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 CardioCard Holter?
The registered manufacturer of record for CardioCard Holter is NASIFF ASSOCIATES INC.
What is the Primary UDI-DI identifier for CardioCard Holter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CUSBHOLTER.
What classification code is assigned to this device?
This device is registered under product classification code DRT.
Similar Classification Devices (DRT)
Other Devices by NASIFF ASSOCIATES INC
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