gudid
Primary ID: EndoTrap
EndoTrap (UDI EndoTrap)
Manufactured by PALLIARE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EndoTrap - Primary ID EndoTrap
Device Regulatory Overview
The EndoTrap (Model/Catalog Number: EndoTrap) is a medical device manufactured by PALLIARE LIMITED. This product is indexed under FDA Product Code / Category Classification FFY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EndoTrap
- Product Code / EMDN
- FFY
- Device Name
- EndoTrap Endoscopist Protection Device
- Database Sync Date
- 2026-08-09 09:57:27
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 EndoTrap?
The registered manufacturer of record for EndoTrap is PALLIARE LIMITED.
What is the Primary UDI-DI identifier for EndoTrap?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EndoTrap.
What classification code is assigned to this device?
This device is registered under product classification code FFY.
Similar Classification Devices (FFY)
Other Devices by PALLIARE LIMITED
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