eudamed_udi
Primary ID: 08058302603544
CREO (UDI 08058302603544)
Manufactured by Malvestio Spa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CREO - Primary ID 08058302603544
Device Regulatory Overview
The CREO (Model/Catalog Number: 348450) is a medical device manufactured by Malvestio Spa. This product is indexed under FDA Product Code / Category Classification V0806010701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 348450
- Product Code / EMDN
- V0806010701
- Device Name
- CREO
- Database Sync Date
- 2026-08-09 16:46:31
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 CREO?
The registered manufacturer of record for CREO is Malvestio Spa.
What is the Primary UDI-DI identifier for CREO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058302603544.
What classification code is assigned to this device?
This device is registered under product classification code V0806010701.
Similar Classification Devices (V0806010701)
Other Devices by Malvestio Spa
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