gudid
Primary ID: Iris CK 2Tone /Red Cat
Iris (UDI Iris CK 2Tone /Red Cat)
Manufactured by INTEROJO INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Iris - Primary ID Iris CK 2Tone /Red Cat
Device Regulatory Overview
The Iris (Model/Catalog Number: Iris CK 2Tone /Red Cat) is a medical device manufactured by INTEROJO INC.. This product is indexed under FDA Product Code / Category Classification LPL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Iris CK 2Tone /Red Cat
- Product Code / EMDN
- LPL
- Device Name
- Database Sync Date
- 2026-08-09 09:09:01
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Iris?
The registered manufacturer of record for Iris is INTEROJO INC..
What is the Primary UDI-DI identifier for Iris?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Iris CK 2Tone /Red Cat.
What classification code is assigned to this device?
This device is registered under product classification code LPL.
Similar Classification Devices (LPL)
Other Devices by INTEROJO INC.
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