gudid
Primary ID: 30900
Fog Guard Anti-Fog Solution with Sponge (UDI 30900)
Manufactured by XODUS MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fog Guard Anti-Fog Solution with Sponge - Primary ID 30900
Device Regulatory Overview
The Fog Guard Anti-Fog Solution with Sponge (Model/Catalog Number: 30900) is a medical device manufactured by XODUS MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification OCT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30900
- Product Code / EMDN
- OCT
- Device Name
- Database Sync Date
- 2026-08-09 09:41:24
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 Fog Guard Anti-Fog Solution with Sponge?
The registered manufacturer of record for Fog Guard Anti-Fog Solution with Sponge is XODUS MEDICAL, INC..
What is the Primary UDI-DI identifier for Fog Guard Anti-Fog Solution with Sponge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30900.
What classification code is assigned to this device?
This device is registered under product classification code OCT.
Similar Classification Devices (OCT)
Other Devices by XODUS MEDICAL, INC.
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