Epidural Anesthesia Kit (UDI 22)
Manufactured by Custom Interventional Pain Management, LLC
Device Regulatory Overview
The Epidural Anesthesia Kit (Model/Catalog Number: 22) is a medical device manufactured by Custom Interventional Pain Management, LLC. This product is indexed under FDA Product Code / Category Classification OGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 22
- Product Code / EMDN
- OGE
- Device Name
- Convenience kit no Lidocaine
- Database Sync Date
- 2026-08-09 09:06:21
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 Epidural Anesthesia Kit?
The registered manufacturer of record for Epidural Anesthesia Kit is Custom Interventional Pain Management, LLC.
What is the Primary UDI-DI identifier for Epidural Anesthesia Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 22.
What classification code is assigned to this device?
This device is registered under product classification code OGE.
Similar Classification Devices (OGE)
Other Devices by Custom Interventional Pain Management, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint