gudid
Primary ID: EPK-I5010
VIDEO PROCESSOR (UDI EPK-I5010)
Manufactured by PENTAX OF AMERICA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIDEO PROCESSOR - Primary ID EPK-I5010
Device Regulatory Overview
The VIDEO PROCESSOR (Model/Catalog Number: EPK-I5010) is a medical device manufactured by PENTAX OF AMERICA, INC.. This product is indexed under FDA Product Code / Category Classification PEA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EPK-I5010
- Product Code / EMDN
- PEA
- Device Name
- VIDEO PROCESSOR (US USED)
- Database Sync Date
- 2026-08-09 09:46:01
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 VIDEO PROCESSOR?
The registered manufacturer of record for VIDEO PROCESSOR is PENTAX OF AMERICA, INC..
What is the Primary UDI-DI identifier for VIDEO PROCESSOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EPK-I5010.
What classification code is assigned to this device?
This device is registered under product classification code PEA.
Similar Classification Devices (PEA)
Other Devices by PENTAX OF AMERICA, INC.
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