eudamed_udi
Primary ID: 08001480010246
LINIDOR TRAVERSA 80x180 (UDI 08001480010246)
Manufactured by Fater S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LINIDOR TRAVERSA 80x180 - Primary ID 08001480010246
Device Regulatory Overview
The LINIDOR TRAVERSA 80x180 (Model/Catalog Number: 8001480010246) is a medical device manufactured by Fater S.p.A.. This product is indexed under FDA Product Code / Category Classification T04010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8001480010246
- Product Code / EMDN
- T04010202
- Device Name
- TRAVERSA
- Database Sync Date
- 2026-08-09 16:51:19
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 LINIDOR TRAVERSA 80x180?
The registered manufacturer of record for LINIDOR TRAVERSA 80x180 is Fater S.p.A..
What is the Primary UDI-DI identifier for LINIDOR TRAVERSA 80x180?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08001480010246.
What classification code is assigned to this device?
This device is registered under product classification code T04010202.
Similar Classification Devices (T04010202)
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