Angiography Contrast Delivery Systems PRESS DUO elite (UDI 04560138482605)
Manufactured by Nemoto Kyorindo Co., Ltd.
Device Regulatory Overview
The Angiography Contrast Delivery Systems PRESS DUO elite (Model/Catalog Number: Many) is a medical device manufactured by Nemoto Kyorindo Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z11039014 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Many
- Product Code / EMDN
- Z11039014
- Device Name
- Angiography Contrast Delivery Systems PRESS DUO elite
- Database Sync Date
- 2026-08-09 18:44:10
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 Angiography Contrast Delivery Systems PRESS DUO elite?
The registered manufacturer of record for Angiography Contrast Delivery Systems PRESS DUO elite is Nemoto Kyorindo Co., Ltd..
What is the Primary UDI-DI identifier for Angiography Contrast Delivery Systems PRESS DUO elite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04560138482605.
What classification code is assigned to this device?
This device is registered under product classification code Z11039014.
Similar Classification Devices (Z11039014)
Other Devices by Nemoto Kyorindo Co., Ltd.
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