eudamed_udi
Primary ID: 03800728497710
Sanplast Citofix (UDI 03800728497710)
Manufactured by Sopharma AD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sanplast Citofix - Primary ID 03800728497710
Device Regulatory Overview
The Sanplast Citofix (Model/Catalog Number: 32003000-0039) is a medical device manufactured by Sopharma AD. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 32003000-0039
- Product Code / EMDN
- M050101
- Device Name
- Sanplast
- Database Sync Date
- 2026-08-09 16:29:31
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 Sanplast Citofix?
The registered manufacturer of record for Sanplast Citofix is Sopharma AD.
What is the Primary UDI-DI identifier for Sanplast Citofix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03800728497710.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Sopharma AD
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