eudamed_udi
Primary ID: 16974523991095
Sterile Wound Compresses (UDI 16974523991095)
Manufactured by CareMax Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sterile Wound Compresses - Primary ID 16974523991095
Device Regulatory Overview
The Sterile Wound Compresses (Model/Catalog Number: 3754 LU/LZ IAN 478577_2504) is a medical device manufactured by CareMax Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification M040204 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3754 LU/LZ IAN 478577_2504
- Product Code / EMDN
- M040204
- Device Name
- Sterile Wound Compresses
- Database Sync Date
- 2026-08-09 16:30:42
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 Sterile Wound Compresses?
The registered manufacturer of record for Sterile Wound Compresses is CareMax Co.,Ltd..
What is the Primary UDI-DI identifier for Sterile Wound Compresses?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16974523991095.
What classification code is assigned to this device?
This device is registered under product classification code M040204.
Similar Classification Devices (M040204)
Other Devices by CareMax Co.,Ltd.
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