gudid
Primary ID: 4500WU
N/A (UDI 4500WU)
Manufactured by PENTAX OF AMERICA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 4500WU
Device Regulatory Overview
The N/A (Model/Catalog Number: 4500WU) is a medical device manufactured by PENTAX OF AMERICA, INC.. This product is indexed under FDA Product Code / Category Classification KLX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4500WU
- Product Code / EMDN
- KLX
- Device Name
- v4.0 CSL WIN10 UPGRADE
- 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 N/A?
The registered manufacturer of record for N/A is PENTAX OF AMERICA, INC..
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4500WU.
What classification code is assigned to this device?
This device is registered under product classification code KLX.
Similar Classification Devices (KLX)
Other Devices by PENTAX OF AMERICA, INC.
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