gudid
Primary ID: 3.0
CAAS MRV (UDI 3.0)
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 MRV - Primary ID 3.0
Device Regulatory Overview
The CAAS MRV (Model/Catalog Number: 3.0) is a medical device manufactured by Pie Medical Imaging B.V.. This product is indexed under FDA Product Code / Category Classification LLZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3.0
- Product Code / EMDN
- LLZ
- Device Name
- Database Sync Date
- 2026-08-09 09:04:29
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 MRV?
The registered manufacturer of record for CAAS MRV is Pie Medical Imaging B.V..
What is the Primary UDI-DI identifier for CAAS MRV?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3.0.
What classification code is assigned to this device?
This device is registered under product classification code LLZ.
Similar Classification Devices (LLZ)
Other Devices by Pie Medical Imaging B.V.
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