gudid
Primary ID: S381650
Otomedics (UDI S381650)
Manufactured by JEDMED INSTRUMENT COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Otomedics - Primary ID S381650
Device Regulatory Overview
The Otomedics (Model/Catalog Number: S381650) 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
- S381650
- Product Code / EMDN
- ETD
- Device Name
- U-Tube 1.35mm ID
- 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 Otomedics?
The registered manufacturer of record for Otomedics is JEDMED INSTRUMENT COMPANY.
What is the Primary UDI-DI identifier for Otomedics?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S381650.
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