gudid
Primary ID: LC4X6EZQ
LAPCORP (UDI LC4X6EZQ)
Manufactured by Asp Global, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LAPCORP - Primary ID LC4X6EZQ
Device Regulatory Overview
The LAPCORP (Model/Catalog Number: LC4X6EZQ) is a medical device manufactured by Asp Global, LLC. This product is indexed under FDA Product Code / Category Classification NNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LC4X6EZQ
- Product Code / EMDN
- NNK
- Device Name
- 4" X 6" PEDIATRIC LED TEST SPECIMEN BAG
- Database Sync Date
- 2026-08-09 09:12:13
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 LAPCORP?
The registered manufacturer of record for LAPCORP is Asp Global, LLC.
What is the Primary UDI-DI identifier for LAPCORP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LC4X6EZQ.
What classification code is assigned to this device?
This device is registered under product classification code NNK.
Similar Classification Devices (NNK)
Other Devices by Asp Global, LLC
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