eudamed_udi
Primary ID: 00749756024396
Kittner Sponge (UDI 00749756024396)
Manufactured by DeRoyal Industries, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kittner Sponge - Primary ID 00749756024396
Device Regulatory Overview
The Kittner Sponge (Model/Catalog Number: 30-101) is a medical device manufactured by DeRoyal Industries, Inc.. This product is indexed under FDA Product Code / Category Classification M040799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30-101
- Product Code / EMDN
- M040799
- Device Name
- Kittner Sponge
- Database Sync Date
- 2026-08-09 16:48:24
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 Kittner Sponge?
The registered manufacturer of record for Kittner Sponge is DeRoyal Industries, Inc..
What is the Primary UDI-DI identifier for Kittner Sponge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00749756024396.
What classification code is assigned to this device?
This device is registered under product classification code M040799.
Similar Classification Devices (M040799)
Other Devices by DeRoyal Industries, Inc.
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