Atlas D-Dimer Latex Kit, 25 Tests (UDI 04260658554959)
Manufactured by Atlas Medical GmbH
Device Regulatory Overview
The Atlas D-Dimer Latex Kit, 25 Tests (Model/Catalog Number: 8.00.17.0.0025) is a medical device manufactured by Atlas Medical GmbH. This product is indexed under FDA Product Code / Category Classification W0103020503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8.00.17.0.0025
- Product Code / EMDN
- W0103020503
- Device Name
- Atlas D-Dimer Latex Kit, 25 Tests
- Database Sync Date
- 2026-08-09 16:28:59
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 Atlas D-Dimer Latex Kit, 25 Tests?
The registered manufacturer of record for Atlas D-Dimer Latex Kit, 25 Tests is Atlas Medical GmbH.
What is the Primary UDI-DI identifier for Atlas D-Dimer Latex Kit, 25 Tests?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260658554959.
What classification code is assigned to this device?
This device is registered under product classification code W0103020503.
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