eudamed_udi
Primary ID: 00195411455423
Odyssey iQ (UDI 00195411455423)
Manufactured by College Park Industries, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Odyssey iQ - Primary ID 00195411455423
Device Regulatory Overview
The Odyssey iQ (Model/Catalog Number: OD iQ LCEN 25 G3) is a medical device manufactured by College Park Industries, Inc.. This product is indexed under FDA Product Code / Category Classification Y062499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OD iQ LCEN 25 G3
- Product Code / EMDN
- Y062499
- Device Name
- MYFOOT1988
- Database Sync Date
- 2026-08-09 16:28:59
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 Odyssey iQ?
The registered manufacturer of record for Odyssey iQ is College Park Industries, Inc..
What is the Primary UDI-DI identifier for Odyssey iQ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00195411455423.
What classification code is assigned to this device?
This device is registered under product classification code Y062499.
Similar Classification Devices (Y062499)
Other Devices by College Park Industries, Inc.
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