gudid
Primary ID: S381584 2
NeoZoline (UDI S381584 2)
Manufactured by JEDMED INSTRUMENT COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoZoline - Primary ID S381584 2
Device Regulatory Overview
The NeoZoline (Model/Catalog Number: S381584 2) is a medical device manufactured by JEDMED INSTRUMENT COMPANY. This product is indexed under FDA Product Code / Category Classification ETD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S381584 2
- Product Code / EMDN
- ETD
- Device Name
- T-Tube 12mm Silicone Pair
- Database Sync Date
- 2026-08-09 09:36:12
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of NeoZoline?
The registered manufacturer of record for NeoZoline is JEDMED INSTRUMENT COMPANY.
What is the Primary UDI-DI identifier for NeoZoline?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S381584 2.
What classification code is assigned to this device?
This device is registered under product classification code ETD.
Similar Classification Devices (ETD)
Other Devices by JEDMED INSTRUMENT COMPANY
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint