gudid
Primary ID: AR102
CORITON (UDI AR102)
Manufactured by CORITON Instrument Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CORITON - Primary ID AR102
Device Regulatory Overview
The CORITON (Model/Catalog Number: AR102) is a medical device manufactured by CORITON Instrument Co.,Ltd. This product is indexed under FDA Product Code / Category Classification FOX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AR102
- Product Code / EMDN
- FOX
- Device Name
- Ventilator Support Arm
- Database Sync Date
- 2026-08-09 09:06:39
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 CORITON?
The registered manufacturer of record for CORITON is CORITON Instrument Co.,Ltd.
What is the Primary UDI-DI identifier for CORITON?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AR102.
What classification code is assigned to this device?
This device is registered under product classification code FOX.
Similar Classification Devices (FOX)
Other Devices by CORITON Instrument Co.,Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint