eudamed_udi
Primary ID: 07798034461067
Subiton NAIL (UDI 07798034461067)
Manufactured by Laboratorios SL S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Subiton NAIL - Primary ID 07798034461067
Device Regulatory Overview
The Subiton NAIL (Model/Catalog Number: 882338) is a medical device manufactured by Laboratorios SL S.A.. This product is indexed under FDA Product Code / Category Classification P09120201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 882338
- Product Code / EMDN
- P09120201
- Device Name
- Clavo endomedular con antibiótico
- Database Sync Date
- 2026-08-09 16:30:05
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 Subiton NAIL?
The registered manufacturer of record for Subiton NAIL is Laboratorios SL S.A..
What is the Primary UDI-DI identifier for Subiton NAIL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07798034461067.
What classification code is assigned to this device?
This device is registered under product classification code P09120201.
Similar Classification Devices (P09120201)
Other Devices by Laboratorios SL S.A.
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