gudid
Primary ID: Noblus
NOBLUS (UDI Noblus)
Manufactured by PENTAX OF AMERICA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NOBLUS - Primary ID Noblus
Device Regulatory Overview
The NOBLUS (Model/Catalog Number: Noblus) is a medical device manufactured by PENTAX OF AMERICA, INC.. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Noblus
- Product Code / EMDN
- IYO
- Device Name
- HITACHI NOBLUS UTRASND PROC W/ SONOELAST
- Database Sync Date
- 2026-08-09 09:15:37
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 NOBLUS?
The registered manufacturer of record for NOBLUS is PENTAX OF AMERICA, INC..
What is the Primary UDI-DI identifier for NOBLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Noblus.
What classification code is assigned to this device?
This device is registered under product classification code IYO.
Similar Classification Devices (IYO)
Other Devices by PENTAX OF AMERICA, INC.
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