gudid
Primary ID: E8C-U8AT-CRT3
LW Scientific, Inc. (UDI E8C-U8AT-CRT3)
Manufactured by LW SCIENTIFIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LW Scientific, Inc. - Primary ID E8C-U8AT-CRT3
Device Regulatory Overview
The LW Scientific, Inc. (Model/Catalog Number: E8C-U8AT-CRT3) is a medical device manufactured by LW SCIENTIFIC, INC.. This product is indexed under FDA Product Code / Category Classification GKG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E8C-U8AT-CRT3
- Product Code / EMDN
- GKG
- Device Name
- USA E8 Combo, Touch-Screen, Test-Tubes & Crits Carriers, 3500, 90-240v
- Database Sync Date
- 2026-08-09 09:17:27
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 LW Scientific, Inc.?
The registered manufacturer of record for LW Scientific, Inc. is LW SCIENTIFIC, INC..
What is the Primary UDI-DI identifier for LW Scientific, Inc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E8C-U8AT-CRT3.
What classification code is assigned to this device?
This device is registered under product classification code GKG.
Similar Classification Devices (GKG)
Other Devices by LW SCIENTIFIC, INC.
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