eudamed_udi
Primary ID: 08053175000322
Herniatome (UDI 08053175000322)
Manufactured by Adria S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Herniatome - Primary ID 08053175000322
Device Regulatory Overview
The Herniatome (Model/Catalog Number: 5091449 R) is a medical device manufactured by Adria S.r.l.. This product is indexed under FDA Product Code / Category Classification A01020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5091449 R
- Product Code / EMDN
- A01020102
- Device Name
- Devices for percutaneous discectomy and motorized for vertebroplasty / kyphoplasty
- Database Sync Date
- 2026-08-09 16:29:36
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 Herniatome?
The registered manufacturer of record for Herniatome is Adria S.r.l..
What is the Primary UDI-DI identifier for Herniatome?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053175000322.
What classification code is assigned to this device?
This device is registered under product classification code A01020102.
Similar Classification Devices (A01020102)
Other Devices by Adria S.r.l.
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