gudid
Primary ID: Orange
NeoGrip (UDI Orange)
Manufactured by Neotech Products LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoGrip - Primary ID Orange
Device Regulatory Overview
The NeoGrip (Model/Catalog Number: Orange) is a medical device manufactured by Neotech Products LLC. This product is indexed under FDA Product Code / Category Classification JAY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Orange
- Product Code / EMDN
- JAY
- Device Name
- The NeoGrip/VersaGrip is intended to organize tubes, cables and circuits.
- Database Sync Date
- 2026-08-09 09:46:41
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 NeoGrip?
The registered manufacturer of record for NeoGrip is Neotech Products LLC.
What is the Primary UDI-DI identifier for NeoGrip?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Orange.
What classification code is assigned to this device?
This device is registered under product classification code JAY.
Similar Classification Devices (JAY)
Other Devices by Neotech Products LLC
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