gudid
Primary ID: 60011178
CanalPro (UDI 60011178)
Manufactured by COLTENE/WHALEDENT INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CanalPro - Primary ID 60011178
Device Regulatory Overview
The CanalPro (Model/Catalog Number: 60011178) is a medical device manufactured by COLTENE/WHALEDENT INC. This product is indexed under FDA Product Code / Category Classification KYX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 60011178
- Product Code / EMDN
- KYX
- Device Name
- CanalPro Syringe Station
- Database Sync Date
- 2026-08-09 09:03:07
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 CanalPro?
The registered manufacturer of record for CanalPro is COLTENE/WHALEDENT INC.
What is the Primary UDI-DI identifier for CanalPro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 60011178.
What classification code is assigned to this device?
This device is registered under product classification code KYX.
Similar Classification Devices (KYX)
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