eudamed_udi
Primary ID: 06942980242466
CANWELL (UDI 06942980242466)
Manufactured by CANWELL MEDICAL CO.,LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CANWELL - Primary ID 06942980242466
Device Regulatory Overview
The CANWELL (Model/Catalog Number: 122292006) is a medical device manufactured by CANWELL MEDICAL CO.,LTD.. This product is indexed under FDA Product Code / Category Classification P09120501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 122292006
- Product Code / EMDN
- P09120501
- Device Name
- Metal Bone Plate
- Database Sync Date
- 2026-08-09 16:30:41
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 CANWELL?
The registered manufacturer of record for CANWELL is CANWELL MEDICAL CO.,LTD..
What is the Primary UDI-DI identifier for CANWELL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942980242466.
What classification code is assigned to this device?
This device is registered under product classification code P09120501.
Similar Classification Devices (P09120501)
Other Devices by CANWELL MEDICAL CO.,LTD.
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