gudid
Primary ID: RT 114
Hybernite RT (UDI RT 114)
Manufactured by Plastiflex Group NV
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hybernite RT - Primary ID RT 114
Device Regulatory Overview
The Hybernite RT (Model/Catalog Number: RT 114) is a medical device manufactured by Plastiflex Group NV. This product is indexed under FDA Product Code / Category Classification BZE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RT 114
- Product Code / EMDN
- BZE
- Device Name
- Hybernite RT 114
- Database Sync Date
- 2026-08-09 09:57:26
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 Hybernite RT?
The registered manufacturer of record for Hybernite RT is Plastiflex Group NV.
What is the Primary UDI-DI identifier for Hybernite RT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RT 114.
What classification code is assigned to this device?
This device is registered under product classification code BZE.
Similar Classification Devices (BZE)
Other Devices by Plastiflex Group NV
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