gudid
Primary ID: CUSB
CardioCard (UDI CUSB)
Manufactured by NASIFF ASSOCIATES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CardioCard - Primary ID CUSB
Device Regulatory Overview
The CardioCard (Model/Catalog Number: CUSB) is a medical device manufactured by NASIFF ASSOCIATES INC. This product is indexed under FDA Product Code / Category Classification DPS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CUSB
- Product Code / EMDN
- DPS
- Device Name
- CardioCard ECG, Stress 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?
The registered manufacturer of record for CardioCard is NASIFF ASSOCIATES INC.
What is the Primary UDI-DI identifier for CardioCard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CUSB.
What classification code is assigned to this device?
This device is registered under product classification code DPS.
Similar Classification Devices (DPS)
Other Devices by NASIFF ASSOCIATES INC
Programmatic Export
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