eudamed_udi
Primary ID: 00849832002079
Thermobrite (UDI 00849832002079)
Manufactured by Leica Biosystems Richmond, Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Thermobrite - Primary ID 00849832002079
Device Regulatory Overview
The Thermobrite (Model/Catalog Number: 3800-004852-001) is a medical device manufactured by Leica Biosystems Richmond, Inc. This product is indexed under FDA Product Code / Category Classification W0299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3800-004852-001
- Product Code / EMDN
- W0299
- Device Name
- Thermobrite
- Database Sync Date
- 2026-08-09 16:46:20
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 Thermobrite?
The registered manufacturer of record for Thermobrite is Leica Biosystems Richmond, Inc.
What is the Primary UDI-DI identifier for Thermobrite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00849832002079.
What classification code is assigned to this device?
This device is registered under product classification code W0299.
Similar Classification Devices (W0299)
Other Devices by Leica Biosystems Richmond, Inc
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