gudid
Primary ID: PD0PP2016
SemiCut Coax. (UDI PD0PP2016)
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 Coax. - Primary ID PD0PP2016
Device Regulatory Overview
The SemiCut Coax. (Model/Catalog Number: PD0PP2016) 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
- PD0PP2016
- Product Code / EMDN
- FCG
- Device Name
- DISPOSABLE SEMIAUTOMATIC GUILLOTINE NEEDLE 20G X 160 mm FOR SOFT TISSUE BIOPSY WITHOUT REMOVABLE LUER, WITH INTRODUCER
- Database Sync Date
- 2026-08-09 09:04:30
Full Regulatory Attributes
🔒 Token Gated
{
"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 Coax.?
The registered manufacturer of record for SemiCut Coax. is M.D.L. S.R.L..
What is the Primary UDI-DI identifier for SemiCut Coax.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PD0PP2016.
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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