eudamed_udi
Primary ID: 00850011135495
VALIDATE (UDI 00850011135495)
Manufactured by LGC Clinical Diagnostics, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VALIDATE - Primary ID 00850011135495
Device Regulatory Overview
The VALIDATE (Model/Catalog Number: 801mm) is a medical device manufactured by LGC Clinical Diagnostics, Inc.. This product is indexed under FDA Product Code / Category Classification W0102152099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 801mm
- Product Code / EMDN
- W0102152099
- Device Name
- VALIDATE® aHBs Test Set
- Database Sync Date
- 2026-08-09 16:49:04
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 VALIDATE?
The registered manufacturer of record for VALIDATE is LGC Clinical Diagnostics, Inc..
What is the Primary UDI-DI identifier for VALIDATE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00850011135495.
What classification code is assigned to this device?
This device is registered under product classification code W0102152099.
Similar Classification Devices (W0102152099)
Other Devices by LGC Clinical Diagnostics, Inc.
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