gudid
Primary ID: Cardiomax
Ascom (UDI Cardiomax)
Manufactured by Ascom (Sweden) AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ascom - Primary ID Cardiomax
Device Regulatory Overview
The Ascom (Model/Catalog Number: Cardiomax) is a medical device manufactured by Ascom (Sweden) AB. This product is indexed under FDA Product Code / Category Classification MSX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Cardiomax
- Product Code / EMDN
- MSX
- Device Name
- Database Sync Date
- 2026-08-09 09:21:51
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Ascom?
The registered manufacturer of record for Ascom is Ascom (Sweden) AB.
What is the Primary UDI-DI identifier for Ascom?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Cardiomax.
What classification code is assigned to this device?
This device is registered under product classification code MSX.
Similar Classification Devices (MSX)
Other Devices by Ascom (Sweden) AB
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint