gudid
Primary ID: PNX2015
MarkX (UDI PNX2015)
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 MarkX - Primary ID PNX2015
Device Regulatory Overview
The MarkX (Model/Catalog Number: PNX2015) is a medical device manufactured by M.D.L. S.R.L.. This product is indexed under FDA Product Code / Category Classification GDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PNX2015
- Product Code / EMDN
- GDF
- Device Name
- NON-REPOSITIONAL DISPOSABLE NEEDLE 20G x 150 mm FOR MAMMARY NODULE LOCALIZATION, WITH DOUBLE HOOK
- Database Sync Date
- 2026-08-09 09:04:28
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 MarkX?
The registered manufacturer of record for MarkX is M.D.L. S.R.L..
What is the Primary UDI-DI identifier for MarkX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PNX2015.
What classification code is assigned to this device?
This device is registered under product classification code GDF.
Similar Classification Devices (GDF)
Other Devices by M.D.L. S.R.L.
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