eudamed_udi
Primary ID: 08056600607929
SPATOLA PER COMPOSITO N.12 TITANIO (UDI 08056600607929)
Manufactured by MEDESY srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPATOLA PER COMPOSITO N.12 TITANIO - Primary ID 08056600607929
Device Regulatory Overview
The SPATOLA PER COMPOSITO N.12 TITANIO (Model/Catalog Number: 509/12T) is a medical device manufactured by MEDESY srl. This product is indexed under FDA Product Code / Category Classification L159013 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 509/12T
- Product Code / EMDN
- L159013
- Device Name
- STRUMENTI CHIRURGICI RIUTILIZZABILI
- Database Sync Date
- 2026-08-09 16:44:54
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 SPATOLA PER COMPOSITO N.12 TITANIO?
The registered manufacturer of record for SPATOLA PER COMPOSITO N.12 TITANIO is MEDESY srl.
What is the Primary UDI-DI identifier for SPATOLA PER COMPOSITO N.12 TITANIO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056600607929.
What classification code is assigned to this device?
This device is registered under product classification code L159013.
Similar Classification Devices (L159013)
Other Devices by MEDESY srl
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