eudamed_udi
Primary ID: 08058090051961
Soffix Trasparent (UDI 08058090051961)
Manufactured by Pikdare S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Soffix Trasparent - Primary ID 08058090051961
Device Regulatory Overview
The Soffix Trasparent (Model/Catalog Number: 58023165000000) is a medical device manufactured by Pikdare S.p.A.. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 58023165000000
- Product Code / EMDN
- M050101
- Device Name
- Soffix Trasparent
- Database Sync Date
- 2026-08-09 16:29:57
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 Soffix Trasparent?
The registered manufacturer of record for Soffix Trasparent is Pikdare S.p.A..
What is the Primary UDI-DI identifier for Soffix Trasparent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058090051961.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Pikdare S.p.A.
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