gudid
Primary ID: Neo12
NeoConnect Oral / Enteral Syringe, OTC (UDI Neo12)
Manufactured by NEOMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoConnect Oral / Enteral Syringe, OTC - Primary ID Neo12
Device Regulatory Overview
The NeoConnect Oral / Enteral Syringe, OTC (Model/Catalog Number: Neo12) is a medical device manufactured by NEOMED, INC.. This product is indexed under FDA Product Code / Category Classification PNR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Neo12
- Product Code / EMDN
- PNR
- Device Name
- 12mL NeoConnect Enteral Syringe with ENFit Connector, Non-Sterile, OTC
- Database Sync Date
- 2026-08-09 09:33:01
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 NeoConnect Oral / Enteral Syringe, OTC?
The registered manufacturer of record for NeoConnect Oral / Enteral Syringe, OTC is NEOMED, INC..
What is the Primary UDI-DI identifier for NeoConnect Oral / Enteral Syringe, OTC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Neo12.
What classification code is assigned to this device?
This device is registered under product classification code PNR.
Similar Classification Devices (PNR)
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