eudamed_udi
Primary ID: 08056304453471
CAAS IntraVascular (UDI 08056304453471)
Manufactured by Pie Medical Imaging B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CAAS IntraVascular - Primary ID 08056304453471
Device Regulatory Overview
The CAAS IntraVascular (Model/Catalog Number: 2.0) is a medical device manufactured by Pie Medical Imaging B.V.. This product is indexed under FDA Product Code / Category Classification Z11039082 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2.0
- Product Code / EMDN
- Z11039082
- Device Name
- CAAS IntraVascular 2.0
- Database Sync Date
- 2026-08-09 18:38:36
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 CAAS IntraVascular?
The registered manufacturer of record for CAAS IntraVascular is Pie Medical Imaging B.V..
What is the Primary UDI-DI identifier for CAAS IntraVascular?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056304453471.
What classification code is assigned to this device?
This device is registered under product classification code Z11039082.
Similar Classification Devices (Z11039082)
Other Devices by Pie Medical Imaging B.V.
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