eudamed_udi
Primary ID: 08032595870197
Cikatridina hüvelykúp (UDI 08032595870197)
Manufactured by FARMA-DERMA S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cikatridina hüvelykúp - Primary ID 08032595870197
Device Regulatory Overview
The Cikatridina hüvelykúp (Model/Catalog Number: 1037) is a medical device manufactured by FARMA-DERMA S.r.l.. This product is indexed under FDA Product Code / Category Classification U0803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1037
- Product Code / EMDN
- U0803
- Device Name
- CICATRIDINA OVULI VAGINALI
- Database Sync Date
- 2026-08-09 16:49:49
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 Cikatridina hüvelykúp?
The registered manufacturer of record for Cikatridina hüvelykúp is FARMA-DERMA S.r.l..
What is the Primary UDI-DI identifier for Cikatridina hüvelykúp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08032595870197.
What classification code is assigned to this device?
This device is registered under product classification code U0803.
Similar Classification Devices (U0803)
Other Devices by FARMA-DERMA S.r.l.
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