gudid
Primary ID: 0088750100
XPERIENCE Advanced Surgical Irrigation (UDI 0088750100)
Manufactured by OSARTIS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for XPERIENCE Advanced Surgical Irrigation - Primary ID 0088750100
Device Regulatory Overview
The XPERIENCE Advanced Surgical Irrigation (Model/Catalog Number: 0088750100) is a medical device manufactured by OSARTIS GmbH. This product is indexed under FDA Product Code / Category Classification FRO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0088750100
- Product Code / EMDN
- FRO
- Device Name
- XPERIENCE Advanced Surgical Irrigation is a clear, colorless solution indicated for cleansing and removal of debris, including microorganisms, from wounds.
- Database Sync Date
- 2026-08-09 09:00:28
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 XPERIENCE Advanced Surgical Irrigation?
The registered manufacturer of record for XPERIENCE Advanced Surgical Irrigation is OSARTIS GmbH.
What is the Primary UDI-DI identifier for XPERIENCE Advanced Surgical Irrigation?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0088750100.
What classification code is assigned to this device?
This device is registered under product classification code FRO.
Similar Classification Devices (FRO)
Other Devices by OSARTIS GmbH
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