eudamed_udi
Primary ID: 08053876007651
LINK IN - Ti Base (UDI 08053876007651)
Manufactured by NEW ANCORVIS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LINK IN - Ti Base - Primary ID 08053876007651
Device Regulatory Overview
The LINK IN - Ti Base (Model/Catalog Number: ILSAILFO35R/N) is a medical device manufactured by NEW ANCORVIS SRL. This product is indexed under FDA Product Code / Category Classification Q010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ILSAILFO35R/N
- Product Code / EMDN
- Q010299
- Device Name
- Link In Tibase
- Database Sync Date
- 2026-08-09 16:28:55
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 LINK IN - Ti Base?
The registered manufacturer of record for LINK IN - Ti Base is NEW ANCORVIS SRL.
What is the Primary UDI-DI identifier for LINK IN - Ti Base?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053876007651.
What classification code is assigned to this device?
This device is registered under product classification code Q010299.
Similar Classification Devices (Q010299)
Other Devices by NEW ANCORVIS SRL
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