gudid
Primary ID: DDP015
LiquiPhil (UDI DDP015)
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 DDP015
Device Regulatory Overview
The LiquiPhil (Model/Catalog Number: DDP015) 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
- DDP015
- Product Code / EMDN
- IXG
- Device Name
- Optional PTW31030 Chamber Mount
- Database Sync Date
- 2026-08-09 09:22:08
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 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 DDP015.
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.
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