gudid
Primary ID: 955516MDR
TherMax (UDI 955516MDR)
Manufactured by Vantive Health GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TherMax - Primary ID 955516MDR
Device Regulatory Overview
The TherMax (Model/Catalog Number: 955516MDR) is a medical device manufactured by Vantive Health GmbH. This product is indexed under FDA Product Code / Category Classification KDI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 955516MDR
- Product Code / EMDN
- KDI
- Device Name
- The Blood Warmer Disposable is a disposable circuit for use with the TherMax blood warmer in combination with other PrisMax disposable sets.
- Database Sync Date
- 2026-08-09 09:10:27
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 TherMax?
The registered manufacturer of record for TherMax is Vantive Health GmbH.
What is the Primary UDI-DI identifier for TherMax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 955516MDR.
What classification code is assigned to this device?
This device is registered under product classification code KDI.
Similar Classification Devices (KDI)
Other Devices by Vantive Health GmbH
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