gudid
Primary ID: P44880
Pilling (UDI P44880)
Manufactured by Avalign Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pilling - Primary ID P44880
Device Regulatory Overview
The Pilling (Model/Catalog Number: P44880) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification FHN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P44880
- Product Code / EMDN
- FHN
- Device Name
- McGivney hemorrhoidal Ligator, Includes Cone and O-Rings, Latex O-Rings, Cone Material is Polyoxymethylene Nature
- Database Sync Date
- 2026-08-09 09:02:38
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 Pilling?
The registered manufacturer of record for Pilling is Avalign Technologies, Inc..
What is the Primary UDI-DI identifier for Pilling?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P44880.
What classification code is assigned to this device?
This device is registered under product classification code FHN.
Similar Classification Devices (FHN)
Other Devices by Avalign Technologies, Inc.
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