gudid
Primary ID: PL
Palium (UDI PL)
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 Palium - Primary ID PL
Device Regulatory Overview
The Palium (Model/Catalog Number: PL) 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
- PL
- Product Code / EMDN
- FCG
- Device Name
- AUTOMATIC REUSABLE GUNFOR SOFT TISSUES BIOPSY,PALIUM TYPE
- Database Sync Date
- 2026-08-09 09:04:30
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 Palium?
The registered manufacturer of record for Palium is M.D.L. S.R.L..
What is the Primary UDI-DI identifier for Palium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PL.
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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