gudid
Primary ID: Mobile Holder HKH 8860
Cardiohelp (UDI Mobile Holder HKH 8860)
Manufactured by Maquet Cardiopulmonary AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cardiohelp - Primary ID Mobile Holder HKH 8860
Device Regulatory Overview
The Cardiohelp (Model/Catalog Number: Mobile Holder HKH 8860) is a medical device manufactured by Maquet Cardiopulmonary AG. This product is indexed under FDA Product Code / Category Classification DTQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Mobile Holder HKH 8860
- Product Code / EMDN
- DTQ
- Device Name
- CARDIOHELP mobile holder model HKH 8860. The CARDIOHELP Mobile Holder is for connecting the CARDIOHELP Base Plate or CARDIOHELP Wall Holder incl. CARDIOHELP protection cover.
- Database Sync Date
- 2026-08-09 09:11:49
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 Cardiohelp?
The registered manufacturer of record for Cardiohelp is Maquet Cardiopulmonary AG.
What is the Primary UDI-DI identifier for Cardiohelp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Mobile Holder HKH 8860.
What classification code is assigned to this device?
This device is registered under product classification code DTQ.
Similar Classification Devices (DTQ)
Other Devices by Maquet Cardiopulmonary AG
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