gudid
Primary ID: 12150000Z
PerFRACTION (UDI 12150000Z)
Manufactured by SUN NUCLEAR CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PerFRACTION - Primary ID 12150000Z
Device Regulatory Overview
The PerFRACTION (Model/Catalog Number: 12150000Z) is a medical device manufactured by SUN NUCLEAR CORP.. This product is indexed under FDA Product Code / Category Classification IYE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12150000Z
- Product Code / EMDN
- IYE
- Device Name
- Radiation therapy QA device.
- Database Sync Date
- 2026-08-09 09:16:43
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 PerFRACTION?
The registered manufacturer of record for PerFRACTION is SUN NUCLEAR CORP..
What is the Primary UDI-DI identifier for PerFRACTION?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12150000Z.
What classification code is assigned to this device?
This device is registered under product classification code IYE.
Similar Classification Devices (IYE)
Other Devices by SUN NUCLEAR CORP.
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