Reusable ENFit Syringe (UDI NEO3)
Manufactured by Avanos Medical, Inc.
Device Regulatory Overview
The Reusable ENFit Syringe (Model/Catalog Number: NEO3) is a medical device manufactured by Avanos Medical, Inc.. This product is indexed under FDA Product Code / Category Classification PNR within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- NEO3
- Product Code / EMDN
- PNR
- Device Name
- 3mL NC at Home ENFit Syringe Reusable
- Database Sync Date
- 2026-08-09 09:20:10
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 Reusable ENFit Syringe?
The registered manufacturer of record for Reusable ENFit Syringe is Avanos Medical, Inc..
What is the Primary UDI-DI identifier for Reusable ENFit Syringe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NEO3.
What classification code is assigned to this device?
This device is registered under product classification code PNR.
Similar Classification Devices (PNR)
Other Devices by Avanos Medical, Inc.
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