gudid
Primary ID: JK2442
DYNAMIC DIAGNOSTICS (UDI JK2442)
Manufactured by Asp Global, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DYNAMIC DIAGNOSTICS - Primary ID JK2442
Device Regulatory Overview
The DYNAMIC DIAGNOSTICS (Model/Catalog Number: JK2442) is a medical device manufactured by Asp Global, LLC. This product is indexed under FDA Product Code / Category Classification ITG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- JK2442
- Product Code / EMDN
- ITG
- Device Name
- COHESIVE BANDAGE 2" X 5 YD MULTI-COLOR LATEX-FREE NON-STERILE (DYNAMIC'S LOGO) , 1/EA,36/CS
- Database Sync Date
- 2026-08-09 09:14:02
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 DYNAMIC DIAGNOSTICS?
The registered manufacturer of record for DYNAMIC DIAGNOSTICS is Asp Global, LLC.
What is the Primary UDI-DI identifier for DYNAMIC DIAGNOSTICS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is JK2442.
What classification code is assigned to this device?
This device is registered under product classification code ITG.
Similar Classification Devices (ITG)
Other Devices by Asp Global, LLC
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