Integra Jarit (UDI 380336)
Manufactured by INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Device Regulatory Overview
The Integra Jarit (Model/Catalog Number: 380336) is a medical device manufactured by INTEGRA LIFESCIENCES PRODUCTION CORPORATION. This product is indexed under FDA Product Code / Category Classification KCJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 380336
- Product Code / EMDN
- KCJ
- Device Name
- Integra Jarit Farrell Applicator, Roughened End
- Database Sync Date
- 2026-08-09 10:01:56
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 Integra Jarit?
The registered manufacturer of record for Integra Jarit is INTEGRA LIFESCIENCES PRODUCTION CORPORATION.
What is the Primary UDI-DI identifier for Integra Jarit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 380336.
What classification code is assigned to this device?
This device is registered under product classification code KCJ.
Similar Classification Devices (KCJ)
Other Devices by INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint