gudid
Primary ID: TLP226
LiquiPhil (UDI TLP226)
Manufactured by Providus Holdings, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LiquiPhil - Primary ID TLP226
Device Regulatory Overview
The LiquiPhil (Model/Catalog Number: TLP226) is a medical device manufactured by Providus Holdings, Inc.. This product is indexed under FDA Product Code / Category Classification IXG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TLP226
- Product Code / EMDN
- IXG
- Device Name
- Additional 2cm x 4cm tumor vessel and support post
- Database Sync Date
- 2026-08-09 09:22:08
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of LiquiPhil?
The registered manufacturer of record for LiquiPhil is Providus Holdings, Inc..
What is the Primary UDI-DI identifier for LiquiPhil?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TLP226.
What classification code is assigned to this device?
This device is registered under product classification code IXG.
Similar Classification Devices (IXG)
Other Devices by Providus Holdings, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint