NeuEra (UDI 06976302230046)
Manufactured by Shenyang Intelligent Neuclear Medical Technology Co., Ltd.
Device Regulatory Overview
The NeuEra (Model/Catalog Number: none) is a medical device manufactured by Shenyang Intelligent Neuclear Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z11020301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- none
- Product Code / EMDN
- Z11020301
- Device Name
- Positron Emission Tomography (PET) and Computed Tomography (CT) System
- Database Sync Date
- 2026-08-09 17:28:23
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 NeuEra?
The registered manufacturer of record for NeuEra is Shenyang Intelligent Neuclear Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for NeuEra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976302230046.
What classification code is assigned to this device?
This device is registered under product classification code Z11020301.
Similar Classification Devices (Z11020301)
Other Devices by Shenyang Intelligent Neuclear Medical Technology Co., Ltd.
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