Vigil Protein Control Level 1 (UDI 15099590226916)
Manufactured by Beckman Coulter Inc.
Device Regulatory Overview
The Vigil Protein Control Level 1 (Model/Catalog Number: 450120) is a medical device manufactured by Beckman Coulter Inc.. This product is indexed under FDA Product Code / Category Classification W0102152003 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 450120
- Product Code / EMDN
- W0102152003
- Device Name
- Vigil Protein Control Level 1
- Database Sync Date
- 2026-08-09 16:30:11
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 Vigil Protein Control Level 1?
The registered manufacturer of record for Vigil Protein Control Level 1 is Beckman Coulter Inc..
What is the Primary UDI-DI identifier for Vigil Protein Control Level 1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15099590226916.
What classification code is assigned to this device?
This device is registered under product classification code W0102152003.
Similar Classification Devices (W0102152003)
Other Devices by Beckman Coulter Inc.
- → SYNCHRON Systems Phosphorus (PHOSm) Reagent REF: 467868 For In Vitro Diagnostic Use, Rx Only.
- → SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent, REF: 969706
- → DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clinical Analyzer
- → UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205,
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