gudid
Primary ID: 12160000
PlanIQ (UDI 12160000)
Manufactured by SUN NUCLEAR CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PlanIQ - Primary ID 12160000
Device Regulatory Overview
The PlanIQ (Model/Catalog Number: 12160000) 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
- 12160000
- Product Code / EMDN
- IYE
- Device Name
- Radiation therapy QA device.
- Database Sync Date
- 2026-08-09 09:16:43
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PlanIQ?
The registered manufacturer of record for PlanIQ is SUN NUCLEAR CORP..
What is the Primary UDI-DI identifier for PlanIQ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12160000.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint