gudid
Primary ID: RLK41U
Vega (UDI RLK41U)
Manufactured by MICROPORT CRM SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vega - Primary ID RLK41U
Device Regulatory Overview
The Vega (Model/Catalog Number: RLK41U) is a medical device manufactured by MICROPORT CRM SRL. This product is indexed under FDA Product Code / Category Classification NVN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RLK41U
- Product Code / EMDN
- NVN
- Device Name
- VEGA Stylet Kit 52cm
- Database Sync Date
- 2026-08-09 09:05:06
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 Vega?
The registered manufacturer of record for Vega is MICROPORT CRM SRL.
What is the Primary UDI-DI identifier for Vega?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RLK41U.
What classification code is assigned to this device?
This device is registered under product classification code NVN.
Similar Classification Devices (NVN)
Other Devices by MICROPORT CRM SRL
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