gudid
Primary ID: PD0PP1810
SemiCut (UDI PD0PP1810)
Manufactured by M.D.L. S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SemiCut - Primary ID PD0PP1810
Device Regulatory Overview
The SemiCut (Model/Catalog Number: PD0PP1810) is a medical device manufactured by M.D.L. S.R.L.. This product is indexed under FDA Product Code / Category Classification FCG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PD0PP1810
- Product Code / EMDN
- FCG
- Device Name
- SEMIAUTOMATIC NEEDLE 18G x 100mmWITHOUT REMOVABLE LUER,WITH INTRODUCER
- Database Sync Date
- 2026-08-09 09:04:32
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 SemiCut?
The registered manufacturer of record for SemiCut is M.D.L. S.R.L..
What is the Primary UDI-DI identifier for SemiCut?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PD0PP1810.
What classification code is assigned to this device?
This device is registered under product classification code FCG.
Similar Classification Devices (FCG)
Other Devices by M.D.L. S.R.L.
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