eudamed_udi
Primary ID: 08059386746295
SURGICAL INSTRUMENTS (IR) (UDI 08059386746295)
Manufactured by Citieffe s.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SURGICAL INSTRUMENTS (IR) - Primary ID 08059386746295
Device Regulatory Overview
The SURGICAL INSTRUMENTS (IR) (Model/Catalog Number: DT072003) is a medical device manufactured by Citieffe s.r.l.. This product is indexed under FDA Product Code / Category Classification L091001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DT072003
- Product Code / EMDN
- L091001
- Device Name
- GUIDE WIRES
- Database Sync Date
- 2026-08-09 16:28:59
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 SURGICAL INSTRUMENTS (IR)?
The registered manufacturer of record for SURGICAL INSTRUMENTS (IR) is Citieffe s.r.l..
What is the Primary UDI-DI identifier for SURGICAL INSTRUMENTS (IR)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08059386746295.
What classification code is assigned to this device?
This device is registered under product classification code L091001.
Similar Classification Devices (L091001)
Other Devices by Citieffe s.r.l.
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