eudamed_udi
Primary ID: 08058302601359
LINKAR (UDI 08058302601359)
Manufactured by Malvestio Spa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LINKAR - Primary ID 08058302601359
Device Regulatory Overview
The LINKAR (Model/Catalog Number: 329633) is a medical device manufactured by Malvestio Spa. This product is indexed under FDA Product Code / Category Classification V0899 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 329633
- Product Code / EMDN
- V0899
- Device Name
- LINKAR
- Database Sync Date
- 2026-08-09 16:30:32
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 LINKAR?
The registered manufacturer of record for LINKAR is Malvestio Spa.
What is the Primary UDI-DI identifier for LINKAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058302601359.
What classification code is assigned to this device?
This device is registered under product classification code V0899.
Similar Classification Devices (V0899)
Other Devices by Malvestio Spa
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