gudid
Primary ID: SR20080-02
SINUREP (UDI SR20080-02)
Manufactured by MEDAX SRL UNIPERSONALE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SINUREP - Primary ID SR20080-02
Device Regulatory Overview
The SINUREP (Model/Catalog Number: SR20080-02) is a medical device manufactured by MEDAX SRL UNIPERSONALE. This product is indexed under FDA Product Code / Category Classification MIJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SR20080-02
- Product Code / EMDN
- MIJ
- Device Name
- Breast localization needle Mod. SINUREP 20G x 80 mm
- Database Sync Date
- 2026-08-09 09:04:28
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 SINUREP?
The registered manufacturer of record for SINUREP is MEDAX SRL UNIPERSONALE.
What is the Primary UDI-DI identifier for SINUREP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SR20080-02.
What classification code is assigned to this device?
This device is registered under product classification code MIJ.
Similar Classification Devices (MIJ)
Other Devices by MEDAX SRL UNIPERSONALE
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