gudid
Primary ID: M21304
Kozee (UDI M21304)
Manufactured by SOURCEMARK, LLC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kozee - Primary ID M21304
Device Regulatory Overview
The Kozee (Model/Catalog Number: M21304) is a medical device manufactured by SOURCEMARK, LLC.. This product is indexed under FDA Product Code / Category Classification DWJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M21304
- Product Code / EMDN
- DWJ
- Device Name
- Extra Large Warming Suit
- Database Sync Date
- 2026-08-09 09:29:36
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 Kozee?
The registered manufacturer of record for Kozee is SOURCEMARK, LLC..
What is the Primary UDI-DI identifier for Kozee?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M21304.
What classification code is assigned to this device?
This device is registered under product classification code DWJ.
Similar Classification Devices (DWJ)
Other Devices by SOURCEMARK, LLC.
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